Appendectomy

8

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

Condition / disease
Location
Status: Not yet recruiting

Hospital Based Continuous Patient Monitoring System

In Ghana, and many other low and middle income countries in Africa, manual vital signs monitoring is the prevalent mode of vital signs monitoring because continuous bedside monitors are non-functional. This lack of continuous vital signs monitoring may result in missed opportunities to catch physiologic deterioration. The investigators propose to develop a dashboard that is based on the Garmin Venu 3, a consumer wearable device that reliably measures heart rate, SPO2, and respiratory rate, as an alternative to bedside monitors in hospitals in Ghana.

Participants needed: 250
Trial details
Age: 3-18Biological sex: AllType: InterventionalSponsor: University of Alabama at BirminghamUpdated: Jul 2, 2026
Eligibility criteria

Pediatric patients presenting with traumatic injury [+1]

Pediatric patients missing their upper limbs, [+1]

Status: Not yet recruiting

Quality of Life and Pain After Appendectomy in Children

Acute appendicitis is one of the most common emergency general surgical conditions worldwide and represents the leading cause of emergency abdominal surgery in children. In some cases, appendectomy may result in persistent or recurrent pain in the right iliac fossa, which may negatively affect quality of life, particularly in children. The primary aim of this study is to determine the prevalence of chronic pain at the third postoperative month in pediatric patients who underwent appendectomy. The age, sex, body mass index, and comorbidities of patients aged 8-18 years who underwent appendectomy will be recorded. Pain in children who met the inclusion criteria was assessed using the Numeric Rating Scale (NRS). To evaluate the effects of pain on quality of life, the child and parent versions of the Pediatric Quality of Life Inventory (PedsQL) were administered at the third postoperative month. In addition, the Functional Disability Inventory (FDI) was used at the third postoperative month to assess the impact of pain on the patient's functional status.

Participants needed: 231
Trial details
Age: 8-18Biological sex: AllType: ObservationalSponsor: Kocaeli City HospitalUpdated: Jun 5, 2026Locations: 1Duration: 3 Months
Eligibility criteria

Not listed

Status: Recruiting

Early Detection of Infection Using the Fitbit in Pediatric Surgical Patients

The purpose of this study is to analyze Fitbit data to predict infection after surgery for complicated appendicitis and the effect this prediction has on clinician decision making.

Participants needed: 500
Trial details
Age: 3-18Biological sex: AllType: InterventionalSponsor: Ann & Robert H Lurie Children's Hospital of ChicagoUpdated: May 13, 2026Locations: 4
Eligibility criteria

children aged 3-18 years [+1]

children who are non-ambulatory or have any pre-existing mobility limitations [+3]

Status: Recruiting

The Effectiveness of Dexmedetomidine as an Adjuvant for Bupivacaine Caudal Block in Pediatric Open Appendectomy Under General Anesthesia

This study aims to evaluate if adding dexmedetomidine to bupivacaine in a caudal block can provide longer and better quality pain relief for children after open appendectomy surgery. The study will also assess the effect of this combination on the quality of recovery, including the incidence of emergence delirium, and its overall safety profile.

Participants needed: 60
Trial details
Age: 2-7Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: May 6, 2026Locations: 1
Eligibility criteria

ASA (American Society of Anesthesiologists) physical status I or II. [+1]

Refusal of participation by the legal guardian. [+7]

Status: Recruiting

Exploring the Impact of Genetic Variations on The Clinical Efficacy of Nalbuphine in Postoperative Pain Management

The goal of this study is to identify the genes as well as their association with Nalbuphine. This will help the investigator to identify opioid vulnerability in Pakistani population in the postoperative patients and will contribute to overcoming the opioid crisis, resulting in better and safer outcomes. Research question is: Is there any association between the underlying genetic variations and the analgesic efficacy of Nalbuphine in postoperative patients? The Research Objectives are 1. To identify the underlying genes in postoperative patients having pain. 2. To find an association between identified genes and nalbuphine clinical efficacy. Procedure: After the written informed consent adult men and women will be enrolled in the study. On the day of surgery in the preoperative area, a 5 ml blood sample will be drawn before surgery and will be sent to laboratory for analysis. After routine hemodynamic monitoring in the operative room, general anesthesia will be given including nalbuphine. Standard routine anesthesia monitoring will be done and maintained while monitoring heart rate, ECG, NIBP oxygen saturation, ETCO2 and temperature. Incremental analgesia will be provided whenever needed. After extubation and shifting to recovery room the 2nd sample of blood will be taken and will be sent for analysis. Pain score, nausea vomiting, sedation, requirement of analgesia will be assessed till 24 hours postoperatively.

Participants needed: 263
Trial details
Phase: Phase 2, Phase 3Age: 18-70Biological sex: AllType: InterventionalSponsor: Dr. Asma Abdus SalamUpdated: Apr 15, 2026Locations: 1
Eligibility criteria

All adult men or women [+3]

Surgical procedure duration lasting more than 4 hours [+7]

Status: Recruiting

Re-assessment of Appendicitis Evaluation During Laparoscopic Appendectomy, Peritoneal Irrigation During Laparoscopic Appendectomy Does the Grade of Contamination Matter?

Type: prospective observational multicenter trial. Population of interest: adult patients undergoing laparoscopic appendectomy for acute appendicitis. Hypothesis : laparoscopic lavage during laparoscopic appendectomy is a practice that should be used in selected patients according to the intraperitoneal grade of contamination and grade of appendicitis. Nonregulated use of laparoscopic lavage cannot be considered superior to suction only considering recent evidence. Few RCT available addressing this issue are available, but any with a high methodological quality. Aim: The aim of this study is to investigate the impact of laparoscopic lavage during laparoscopic appendectomy on the postoperative incidence of intrabdominal abscesses, stratifying patients in different clusters according to a defined classification considering the intraperitoneal contamination and grade of appendicitis.

Participants needed: 1,067
Trial details
Age: 18-69Biological sex: AllType: ObservationalSponsor: Niguarda HospitalUpdated: Apr 16, 2026Locations: 1
Eligibility criteria

Patients between 18 and 69 years old [+2]

Patients < 18 years old or > 69 years old [+6]

Status: Recruiting

Comparison Of Clinical Outcomes of Intraperitoneal Bupivacaine Instillation Versus Placebo as Preemptive Analgesia in Patients Undergoing Open Appendectomy

To compare the clinical outcomes of intraperitoneal bupivacaine instillation vs placebo as preemptive analgesia in patients undergoing open appendectomy

Participants needed: 60
Trial details
Phase: Phase 1Age: 20-60Biological sex: AllType: InterventionalSponsor: Sardar Umer RehmanUpdated: Feb 24, 2026Locations: 1
Eligibility criteria

Patients presenting to the emergency department undergoing open appendectomy.

Patients undergoing interval appendectomy or having perforated appendix as evide... [+7]

Status: Recruiting

A Global Prospective Cohort Study on Outcomes of Appendicectomy for Appendicitis

This study aims to assess and improve the global management of appendicitis, the most common emergency surgery, by examining various aspects of emergency care systems worldwide. Appendicitis is a time-sensitive condition, and delays in diagnosis or treatment can lead to complications, affecting patient outcomes and increasing healthcare costs. The study uses appendicitis as a "tracer condition" to explore how different healthcare systems manage emergency care, focusing on factors like access, quality, and efficiency. By gathering data from hospitals worldwide, the study seeks to identify areas where emergency surgical care can be improved, particularly in low- and middle-income countries (LMICs). The main goal is to identify gaps in emergency care systems, using a set of key performance measures (KPMs) that assess access to care, the quality of surgical treatment, and patient safety. These include factors like the time from symptom onset to first surgical assessment, the rate of appendectomy performed via minimally invasive (laparoscopic) surgery, and postoperative complications. The study aims to collect data on at least 14,000 patients from around 500 hospitals globally between February and May 2025. The data will be analyzed by hospital income group (from low to high) to understand how different resource levels impact outcomes and to help guide future policy and practice improvements. The study also includes two sub-studies that focus on specific issues in surgical care. The Sustainability and Waste Management sub-study aims to explore how hospitals manage waste and sustainability practices in operating theatres. This sub-study is part of global efforts to reduce carbon emissions in healthcare settings. The Financing sub-study examines the financial burden of appendicectomy, particularly the out-of-pocket costs for patients in LMICs. It will explore how the costs of open vs. laparoscopic surgery differ and investigate the impact of these costs on patients. By combining global data on clinical outcomes with information on hospital resources and patient finances, this study hopes to provide valuable insights into how to improve emergency surgical care across diverse settings, making recommendations that can lead to better access to safe, timely, and affordable treatment for appendicitis worldwide.

Participants needed: 14,000
Trial details
Biological sex: AllType: ObservationalSponsor: University of BirminghamUpdated: Apr 2, 2025Locations: 7Duration: 30 Days
Eligibility criteria

Age: There are no age restrictions, although, if appropriate participating hospi... [+2]

Indication: Appendicectomy for any indication other than suspected or confirmed... [+4]