Status:
RECRUITING
Comparison the Analgesic Efficacy of Ultrasonographic Bilateral TAP and Anesthetic Infiltration Into the Surgery Field for Laparoscopic Unilateral TEP Herniorrhaphy
Lead Sponsor:
Başakşehir Çam & Sakura City Hospital
Conditions:
Laparoscopic Surgery
Herniorrhaphy
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
Laparoscopic inguinal hernia repair is a common surgical procedure, but postoperative pain management remains a challenge. This prospective, randomized study aims to compare the analgesic efficacy of ...
Detailed Description
Abdominal fascial plane blocks are now considered adequate and reliable methods for the management of postoperative pain following both open and laparoscopic abdominal procedures. Abdominal fascial pl...
Eligibility Criteria
Inclusion
- Consenting patients,
- She will undergo laparoscopic hernia repair surgery,
- ASA-I-II,
- Between the ages of 18 and 65,
- No history of anticoagulant or antiaggregant drug use,
- Regional anesthesia is not contraindicated and the anesthesiologist deems -appropriate for regional anesthesia,
- Under general anesthesia and will undergo laparoscopic surgery,
- Fully oriented and cooperative,
- Unilateral inguinal hernia,
- No previous surgery for inguinal hernia,
- No incision in the lower abdomen,
- Not using alcohol and drugs,
- No preoperative pain and
- Patients without symptoms of strangulated hernia will be included in the study.
Exclusion
- Patients without consent
- Regional anesthesia is contraindicated,
- Those who will undergo open abdominal surgery,
- Not in the appropriate age range,
- Chronic diseases such as uncontrolled DM and HT,
- Drug allergy,
- Taking anticoagulant or antiaggregant drugs,
- History of chronic analgesic use,
- Presence of active infection in the area to be blocked,
- Will not be able to comply with postoperative pain /VAS follow-up,
- Patients with ASA-III-IV,
- Patients with bilateral inguinal and scrotal hernias,
- Patients who have been previously operated for inguinal hernia and have an incision in the lower abdomen,
- Those with a history of alcohol and drug abuse
- Preoperative pain and
- Those with symptoms of strangulated hernia will not be included in this study.
Key Trial Info
Start Date :
September 4 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 30 2026
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT06894420
Start Date
September 4 2025
End Date
June 30 2026
Last Update
September 24 2025
Active Locations (1)
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1
Başakşehir Çam ve Sakura Şehir Hastanesi
Başakşehir, Istanbul, Turkey (Türkiye), 34480