NCT07101835Completed
EOIB for Laparoscopic Sleeve Gastrectomy
Extent of Sensory Blockade After External Oblique Intercostal Block for Postoperative Analgesia in Laparoscopic Sleeve Gastrectomy
Source: ClinicalTrials.gov · Last updated 23 Dec 2025
Brief summary (registry, in English)
n obese patients, adequate pain relief in the postoperative period is a crucial parameter that affects patient comfort and hospital stay. Improving patient comfort and recovery quality can be achieved by minimizing undesirable effects such as nausea, vomiting, and inadequate analgesia. This study aimed to evaluate the impact of the external oblique intercostal block on postoperative dermatomal distribution, acute pain scores, and opioid consumption during the first 24 hours after laparoscopic sleeve gastrectomy surgery.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 20 (actual)
- First submitted
- 28 Jul 2025
- Start date
- 1 Aug 2025
- Primary completion date
- 1 Nov 2025
- Lead sponsor
- Ondokuz Mayıs University
- Diseases
- Obesity
- NCT number
- NCT07101835
What you commit to
- Study type: Observational
- Participants enrolled: 20
- From 1 Aug 2025 to the primary completion date, 1 Nov 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients with alcohol or drug addiction
Other illness
- Patients with a history of opioid use lasting longer than four weeks
- Patients with a history of allergy or hypersensitivity to local anesthetics or opioids
- Presence of severe cardiac, hepatic, or renal disease
- Conditions contraindicating the application of regional anesthesia
- Patients with severe psychiatric disorders such as psychosis or dementia that limit cooperation
- Block failure identified by dermatomal examination after the procedure
Other
- Patients who did not sign the informed consent form and did not wish to participate in the study
- Patients with chronic pain
- Patients with a STOP-BANG score \> 5
Who the study is looking for
- 18-65 years
Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Ondokuz Mayis University Coordinator of this site? Confirm its status | Samsun | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.