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Clinical Trials in Italy / NCT07051499
Active, not recruiting Observational

Effectiveness of TAP Block Versus Intravenous Analgesia in Postoperative Pain Management Following Gynecologic Laparoscopic Surgery

NCT07051499 · tracked via the Priya Life Science Italy tracker
Sponsor
University of Foggia
Phase
Observational
Started
2025-01-21
Last updated
2025-07-04

Condition(s) studied

Postoperative Pain

Investigational drug(s) / intervention(s)

TAP Block Group

TAP Block Group: Bilateral ultrasound-guided TAP block with 0.25% levobupivacaine and 75 mcg clonidine per side, plus standard intraoperative intravenous analgesia (ketorolac, tramadol, ondansetron).

Study summary

Optimal postoperative pain control is crucial in laparoscopic gynecologic surgery, particularly within Enhanced Recovery After Surgery (ERAS) protocols. The transversus abdominis plane (TAP) block is a regional anesthesia technique that may reduce opioid consumption and enhance recovery. However, data comparing TAP block directly with standard intravenous analgesia in this surgical context are limited.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * age \> 18 years, scheduled for elective gynecological surgery Exclusion Criteria: * age \<18, emergency surgery

Primary outcome measure(s)

  • Postoperative pain intensity (Numeric Rating Scale) — 1, 6, 24 hours postoperatively.
    Postoperative pain will be assessed using the 11-point Numeric Rating Scale (NRS), where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate worse pain. Pain scores will be recorded at 1, 6, and 24 hours postoperatively.

Trial sites (1)

FacilityCityRegionStatus
Policlinico di Foggia Foggia Apulia

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Other trials for the same condition

Temporary Application of Abdominal Jackson-Pratt Drain to Reduce Pain After Laparoscopic Surgery in Gynecology Starting soon
Pain Control After Aortic EndoaneurYsmEctomy (POPEYE) Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07051499 on ClinicalTrials.gov ↗ ← All trials in Italy