Clinical trials

5

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Effect of Preoperative Erector Spinae Plane Block on Recovery Quality, Time to Return to Daily Activities, and Postoperative Pain Scores in Inguinal Hernia Surgery

This study aims to evaluate the effect of the erector spinae plane block (ESPB), performed after surgery, on quality of recovery, postoperative pain, and time to return to daily activities in patients undergoing open inguinal hernia repair under spinal anesthesia. Postoperative pain following inguinal hernia surgery may delay recovery and negatively affect patients' return to normal daily life. Although ESPB has been widely used as an effective analgesic technique in various surgical procedures, its effectiveness in inguinal hernia repair remains limited and not well established. In this randomized controlled study, patients will be divided into two groups: one group will receive ESPB after surgery, while the control group will not receive any block. All patients will receive standard postoperative analgesia. Quality of recovery, acute pain scores, and analgesic consumption will be assessed within the first 24 hours after surgery, and return to daily activities will be evaluated 30 days after surgery. The primary outcome of this study is quality of recovery assessed using the Quality of Recovery-15 (QoR-15) questionnaire. QoR-15 scores range from 0 to 150, with higher scores indicating better recovery. Scores will be recorded preoperatively and 24 hours after surgery. Secondary outcomes include postoperative pain intensity, total opioid consumption, and time to return to daily activities. Pain intensity will be assessed using the Numeric Rating Scale (NRS), where 0 indicates no pain and 10 indicates the worst pain imaginable, at 15, 30, 60, and 120 minutes, as well as 6, 12, and 24 hours after surgery. Total opioid consumption will be determined by recording the cumulative dose of intravenous tramadol administered as rescue analgesia within the first 24 hours after surgery. Time to return to daily activities will be evaluated via telephone follow-up 30 days after surgery.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Sanliurfa Education and Research HospitalUpdated: Jul 2, 2026Locations: 2
Eligibility criteria

Patients aged between 18 and 65 years [+2]

Patients with coagulation disorders [+6]

Status: Not yet recruiting

Comparison of the Effects of External Oblique Intercostal Plane Block and Subcostal Transversus Plane Block Methods With Ultrasound Guidance on Postoperative Analgesia in Laparoscopic Sleeve Gastrectomy Operations

The primary aim of this study was to investigate the effects of the external oblique intercostal plane block and the subcostal transversus abdominis plane block on postoperative pain scores and opioid consumption in patients undergoing laparoscopic sleeve gastrectomy.

Participants needed: 90
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Sanliurfa Education and Research HospitalUpdated: Apr 23, 2026Locations: 1
Eligibility criteria

Adult patients aged between 18 and 65 years [+1]

Patients younger than 18 years or older than 65 years [+4]

Status: Not yet recruiting

Clinical Outcomes After Laser Hemorrhoidoplasty

This single-center prospective observational study aims to evaluate clinical outcomes, postoperative pain scores, complications, and patient satisfaction in adults undergoing laser hemorrhoidoplasty for symptomatic internal hemorrhoidal disease. Additional objectives are to assess the relationship between hemorrhoid stage, dominant presenting symptoms, operative technical details, and postoperative outcomes. No study-specific intervention beyond routine clinical care and follow-up will be performed.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Sanliurfa Education and Research HospitalUpdated: Apr 9, 2026Locations: 1
Eligibility criteria

Age 18 years or older [+3]

Grade IV hemorrhoidal disease [+4]

Status: Recruiting

Comparison of Diagnostic Methods in Patients Operated for Suspected Appendicitis

Acute appendicitis is one of the most common surgical emergencies, but diagnostic uncertainty may still lead to unnecessary appendectomy in some patients. This prospective observational study aims to evaluate the diagnostic performance of computed tomography (CT) reporting and the Appendicitis Inflammatory Response (AIR) score in adult patients undergoing appendectomy for suspected acute appendicitis. The primary objective is to determine the negative appendectomy rate based on final histopathology. Secondary objectives are to assess the agreement between AIR score, CT findings, intraoperative severity grading, and pathology results, and to explore diagnostic performance across patient subgroups. No study-specific intervention beyond routine clinical care will be performed.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Sanliurfa Education and Research HospitalUpdated: Apr 1, 2026Locations: 1
Eligibility criteria

Age 18 years or older [+5]

Age younger than 18 years [+4]

Status: Not yet recruiting

Prediction of Adhesion by Sliding Sign

Sliding sign will be checked by ultrasonography by transabdominal and transvaginal route before operation of patients that had cesarean section three or more. During cesarean section adhesions will be evaluated and noted. The correlation and predictive values of adhesion and sliding sign will be defined in our study.

Participants needed: 100
Trial details
Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Sanliurfa Education and Research HospitalUpdated: Feb 24, 2025
Eligibility criteria

all three and above number of cesarean section patients