Ectopic Pregnancy

13

Review clinical trials related to Ectopic Pregnancy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Letrozole Versus Methotrexate for Management of Undisturbed Ectopic Pregnancy

The aim of work is to study the effectiveness of letrozole in treatment of early undisturbed ectopic pregnancy in comparison with Methotrexate.

Participants needed: 70
Trial details
Phase: Phase 2Age: 20-35Biological sex: FemaleType: InterventionalSponsor: Kafrelsheikh UniversityUpdated: Jun 3, 2026Locations: 1
Eligibility criteria

Confirmed ectopic pregnancy on trans vaginal ultrasound [+4]

Presence of fetal heart pulsation [+5]

Status: Recruiting

Randomized Study of a Dematerialized Management for Post-Emergency Gynecological Follow-Up

The GYNAB study aims to compare patient satisfaction and clinical outcomes between dematerialized post-emergency gynecological follow-up using a connected health app and traditional in-person follow-up. Conducted by Drs. Laëtitia CAMPIN and Louis MARCELLIN at Hôpital Cochin, it is sponsored by Assistance Publique - Hôpitaux de Paris. The main objective is to assess patient satisfaction at day 7 on a scale from 0 to 10, considering symptom management, follow-up quality, and task performance. Secondary objectives include comparing satisfaction at day 28, PROM-ED scores for symptom relief, understanding, reassurance, and care planning at days 7 and 28, hospitalization rates, unscheduled consultations, surgical interventions, total hospital time by day 28, and physician satisfaction at 28 days. This randomized trial involves women aged 18-60 needing follow-up for conditions like genital infections, non-complicated ectopic pregnancies, unlocated pregnancy, first trimester metrorrhagia, miscarriages , and severe vomiting before 12 weeks. Inclusion criteria are women aged 18-60 needing specified follow-up. Exclusion criteria are severe clinical intolerance, severe criteria ultrasound findings, non-French speakers, and inability to use digital applications. The intervention group uses a connected health app for data collection and communication, logging symptoms and test results, with medical team notifications for urgent updates. The control group receives traditional in-person follow-up with scheduled consultations and emergency contact information. The study hypothesizes that digital follow-up will improve patient experience, reduce hospital visits, and provide comparable or superior satisfaction and clinical outcomes. The results could promote broader digital health adoption in various medical fields.

Participants needed: 200
Trial details
Age: 18-60Biological sex: FemaleType: InterventionalSponsor: Assistance Publique - Hôpitaux de ParisUpdated: Apr 21, 2026Locations: 1
Eligibility criteria

Women aged 18 and 60 years [+7]

Signs of severe sepsis with unstable hemodynamics (TA with SBP < 90 mmHg and FC... [+12]

Status: Recruiting

Doppler Flow in Tubal Ectopic Pregnancy in Diagnosis as a Predictor of Treatment Success - Conservative and MTX Treatment

The study "Doppler Flow in Tubal Ectopic Pregnancy as a Predictor of Treatment Success: Conservative and MTX Therapy" aims to evaluate the role of Doppler ultrasound parameters (RI, PI, and PSV) in predicting treatment success for tubal ectopic pregnancies. Ectopic pregnancies, affecting \~2% of all pregnancies (98% in fallopian tubes), pose significant risks, including rupture and maternal mortality. Diagnosis is typically achieved via transvaginal ultrasound, with Doppler imaging enhancing accuracy by detecting characteristic vascular patterns. Management options include conservative monitoring, methotrexate (MTX) therapy, or surgery, based on clinical stability, β-hCG levels, and ultrasound findings. While β-hCG levels are a known predictor of MTX treatment failure, there is no consensus on an optimal threshold. Prior research suggests increased vascularization on Doppler ultrasound may correlate with higher MTX success rates. This prospective study will involve 60 women aged 18-45 with stable, unruptured tubal ectopic pregnancies. It will assess Doppler parameters and other clinical factors as predictors of treatment success. Findings aim to address gaps in the literature and improve management strategies for tubal ectopic pregnancies.

Participants needed: 60
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: Meir Medical CenterUpdated: Apr 21, 2026Locations: 1Duration: 2 Months
Eligibility criteria

Tubal ectopic pregnancy [+2]

Intrauterine pregnancy [+3]

Status: Not yet recruiting

Reproductive Health Education, Birth Control and Sexual Quality of Life in Ectopic Pregnancy

Ectopic pregnancy (EP) is defined as the implantation of a fertilized ovum outside the uterine cavity, most commonly in the fallopian tubes. EP is a potentially life-threatening condition due to the risk of tubal rupture and intra-abdominal bleeding. Management of ectopic pregnancy may involve medical or surgical treatment, often requiring hospitalization. Following treatment and discharge, women may experience physical, emotional, and sexual health challenges. In addition, the need for effective contraception after ectopic pregnancy treatment is critical due to the risk of recurrent ectopic pregnancy and the potential teratogenic effects of treatment agents such as methotrexate. However, limited data are available regarding contraceptive intentions and sexual quality of life after ectopic pregnancy treatment in Türkiye. This study aims to evaluate contraceptive intention and sexual quality of life in women treated for ectopic pregnancy and to examine the relationship between length of hospital stay, contraceptive intention, and sexual quality of life. Data will be collected using the Participant Information Form, the Contraceptive Intention Scale (CIS), and the Sexual Life Quality Scale-Women (SLQS-W). In addition, a reproductive health educational brochure will be provided to participants as part of post-treatment counseling.

Participants needed: 102
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Buket KömürcüUpdated: Feb 24, 2026
Eligibility criteria

Women admitted to the Obstetrics and Gynecology clinics at Izmir City Hospital, [+4]

Women undergoing infertility treatment, [+1]

Status: Recruiting

Posttraumatic Stress Disorder in Ectopic Pregnancy

The objective of the study is to prospectively assess the prevalence of post-traumatic stress disorder (PTSD) symptoms in a population of women who have experienced a diagnosis of ectopic pregnancy. The investigation into the prevalence of PTSD symptoms will aid in better identifying women who may benefit from early psychological intervention.

Participants needed: 200
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: Jagiellonian UniversityUpdated: Dec 29, 2025Locations: 2
Eligibility criteria

ectopic pregnancy [+1]

heterotopic pregnancy

Status: Recruiting

Methotrexate Treatment in Cases of Ectopic Pregnancy With Relative Contraindications

Study Description (For Patients, Families, and Healthcare Providers) Purpose: The aim of this study is to evaluate the effectiveness and safety of methotrexate treatment in women with ectopic pregnancy who belong to a group for whom this treatment is relatively contraindicated. Background: Methotrexate is a medication commonly used in the treatment of ectopic pregnancy (a pregnancy that occurs outside the uterus, usually in the fallopian tube). However, in certain conditions - such as kidney or liver dysfunction - methotrexate use may carry increased risks. These situations are known as relative contraindications. This study will retrospectively examine treatment outcomes in this specific patient population. Method: The study will analyze medical records of patients who were previously treated with methotrexate for ectopic pregnancy. No new interventions will be performed. The analysis will be based solely on existing clinical data. Why Is This Important? The findings of this study may help us better understand the safety limits of methotrexate therapy and guide healthcare providers in managing similar cases in the future.

Participants needed: 230
Trial details
Age: 18-48Biological sex: FemaleType: ObservationalSponsor: Bagcilar Training and Research HospitalUpdated: Sep 22, 2025Locations: 1
Eligibility criteria

Diagnosed with ectopic pregnancy [+3]

Participants with contraindications to methotrexate (MTX) treatment [+1]

Status: Recruiting

Comparison of vNOTES and Laparoscopic Salpingectomy in the Surgical Treatment of Ectopic Pregnancy

This study compares vNOTES salpingectomy and laparoscopic salpingectomy in the treatment of ectopic pregnancy, focusing on outcomes such as operative time, postoperative pain, and recovery.

Participants needed: 56
Trial details
Age: 18-55Biological sex: FemaleType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Aug 5, 2025Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Nalbuphine Dosing and Its Impact on Anxiety and Depression in Ectopic Pregnancy Surgery

This prospective, randomized, controlled study aims to evaluate the impact of different doses of nalbuphine on anxiety and depression in patients undergoing surgery for ectopic pregnancy. Ectopic pregnancy, which occurs in approximately 2% of all pregnancies, often requires surgical intervention, leading to potential psychological distress such as anxiety and depression in affected women. Effective postoperative pain management is essential to enhance recovery and reduce emotional disturbances. The study will involve 165 eligible patients diagnosed with ectopic pregnancy at Jinjiang District Maternal and Child Health Hospital. Participants will be randomly assigned to three groups, each receiving a different concentration of nalbuphine combined with metoclopramide for postoperative analgesia. The primary outcome will focus on changes in anxiety and depression scores measured on postoperative day three, while secondary outcomes will assess pain levels, the use of patient-controlled analgesia (PCA), the necessity for rescue analgesics, and the occurrence of adverse reactions. Sample size calculations suggest that at least 165 participants are required to achieve adequate statistical power. Data will be analyzed using SPSS 25.0 software, with results expected to provide insights into the effectiveness of nalbuphine in improving postoperative recovery and mental health in women experiencing ectopic pregnancy. The study has received ethical approval and is funded by the Chengdu Medical Research Projects (No. 2023465, 2022548, and 2023304).

Participants needed: 165
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Chengdu Jinjiang Maternity and Child Health HospitalUpdated: Jun 8, 2025
Eligibility criteria

Confirmed diagnosis of ectopic pregnancy, aged ≥18 years, and with normal psycho... [+3]

Patients using other analgesic methods or multiple analgesic approaches. [+4]

Status: Not yet recruiting

Psychatric Effect of Ectopic Pregnancy

Assessment of anxiety,depressive symptoms and post traumatic stress after ectopic pregnancy Determine factors associated with development of anxiety,depressive symptoms and post-traumatic stress after ectopic pregnancy

Participants needed: 85
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: Assiut UniversityUpdated: Dec 6, 2024
Eligibility criteria

All pregnant woman 18:45 years old presented with ectopic pregnancy.

intrauterine pregnancy [+2]

Status: Not yet recruiting

Chromotubation on the Remaining Fallopian Tube After a Laparoscopic Salpingectomy Due to Tubal Pregnancy

Ectopic pregnancy prevalence is approximately 1-2% of all pregnancies, majority of which located in the fallopian tube. Among the risk factors for ectopic pregnancy is tubal factor - meaning a mechanical problem within the fallopian tube resulting in the pregnancy remaining in the fallopian tube. The treatment o tubal pregnancy can be expectant, medical via metotrexate or surgicl via laparoscopic salpingectomy of the involved fallopian tube. The purpose of this study is to assess the feasibility of chromotubation during laparoscopic salpingectomy for the surgical management of tubal ectopic pregnancy hence assessing the function of the remaining fallopian tube and trying to predict future fertility for the patient.

Participants needed: 100
Trial details
Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Assaf-Harofeh Medical CenterUpdated: Oct 8, 2024
Eligibility criteria

Patients with a history of unilateral salpingectomy [+2]

Status: Not yet recruiting

Novel Diagnosis of Ectopic Pregnancy

In the project, the investigators aim to determine the Beta- human chorionic gonadotropin (BHCG) value with serial measurements on the same day in the diagnosis of ectopic pregnancy.

Participants needed: 20
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Acibadem UniversityUpdated: Jul 3, 2024
Eligibility criteria

Positive bhcg levels

clinically diagnosis of intrauterine pregnancy

Status: Recruiting

The Effect of Different Treatment Modalities of Tubal Ectopic Pregnancy on Ovarian Reserve: a Prospective Cohort Study

Detect the effect of different treatment modalities of tubal ectopic pregnancy on ovarian reserve

Participants needed: 90
Trial details
Age: 18-44Biological sex: FemaleType: ObservationalSponsor: Assiut UniversityUpdated: Jun 24, 2024Locations: 1
Eligibility criteria

The study will include patients aged 18-44 years with known diagnosis or suspici... [+1]

The use of hormonal contraceptives within two months of enrolment [+3]

Status: Recruiting

Use of Letrozole for Ectopic Pregnancy

A randomized clinical trial using oral letrozole 10mg/day for 7 days, for treating early cases of ectopic pregnancy, compared to intramuscular methotrexate

Participants needed: 130
Trial details
Phase: Phase 4Age: 18+Biological sex: FemaleType: InterventionalSponsor: Hospital de Clinicas de Porto AlegreUpdated: Apr 9, 2024Locations: 1
Eligibility criteria

18 years or older [+9]

Presence of a significant amount of free fluid in the pelvis (as assessed by the... [+8]