NCT07276646 Perioperative Opioid-sparing Effect of Retrosuperior Costotransverse Ligament Block Versus Erector Spinae Block in Laparoscopic Cholecystectomy
| NCT ID | NCT07276646 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Zagazig University |
| Condition | Perioperative Analgesia |
| Study Type | INTERVENTIONAL |
| Enrollment | 80 participants |
| Start Date | 2025-12-10 |
| Primary Completion | 2026-06-10 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 80 participants in total. It began in 2025-12-10 with a primary completion date of 2026-06-10.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
This study aims to compare the analgesic effect of retro superior costotransverse ligament space block vs erector spinae plane block to Achieve high-quality perioperative opioid-sparing effect and postoperative analgesia after laparoscopic cholecystectomy with optimum hemodynamic stability and high patient and surgeon satisfaction
Eligibility Criteria
Inclusion Criteria: 1. patient acceptance 2. Age: 21-64 years old. 3. Sex: both sexes. 4. Physical status: ASA I \& II. 5. Body mass index (BMI): 18.5 - 30 kg/m2. 6. Type of operations: elective laparoscopic cholecystectomy. 7. Duration of surgery not more than 2 hours. Exclusion Criteria: 1. Known hypersensitivity to lidocaine or bupivacaine. 2. Patients with respiratory insufficiency. 3. Coagulation disorders or taking drugs affect surgical hemostasis. 7\. Patients with pre-existing neurological deficits. 8. Uncooperative patient or with altered mental status. 9. Patient with advanced cardiovascular or respiratory diseases
Contact & Investigator
Dina Salem, MD
📞 01099333513
Frequently Asked Questions
Who can join the NCT07276646 clinical trial?
This trial is open to participants of all sexes, aged 21 Years or older, up to 64 Years, studying Perioperative Analgesia. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07276646 currently recruiting?
Yes, NCT07276646 is actively recruiting participants. Visit ClinicalTrials.gov or contact Zagazig University to inquire about joining.
Where is the NCT07276646 trial being conducted?
This trial is being conducted at Zagazig, Egypt.
Who is sponsoring the NCT07276646 clinical trial?
NCT07276646 is sponsored by Zagazig University. The trial plans to enroll 80 participants.