Clonidine in Ultrasound-guided Rectus Sheath Block for Outpatient Umbilical Hernioplasty

PHASE2/PHASE3RecruitingINTERVENTIONAL
Enrollment

62

Participants

Timeline

Start Date

January 7, 2025

Primary Completion Date

December 16, 2025

Study Completion Date

April 30, 2026

Conditions
Hernia, UmbilicalClonidinePain, PostoperativeAmbulatory Surgical ProceduresRegional Anesthesia Block
Interventions
DRUG

Rectus Sheath Block

Participants in this arm will receive bilateral ultrasound-guided rectus sheath block (RSB) with a solution containing 8 mL of lidocaine 2% + 8 mL of ropivacaine 1%, diluted in 0.9% saline to a total volume of 20 mL, each side, without the addition of clonidine.

DRUG

Rectus Sheath Block with Clonidine

Participants in this arm will receive bilateral ultrasound-guided rectus sheath block (RSB) with a solution containing 8 mL of lidocaine 2% + 8 mL of ropivacaine 1% + clonidine 75 mcg, diluted in 0.9% saline to a total volume of 20 mL, each side, without the addition of clonidine.

Trial Locations (1)

20950-003

RECRUITING

Policlinica Universitária Piquet Carneiro, Rio de Janeiro

All Listed Sponsors
lead

Universidade Federal do Rio de Janeiro

OTHER

NCT07062497 - Clonidine in Ultrasound-guided Rectus Sheath Block for Outpatient Umbilical Hernioplasty | Biotech Hunter | Biotech Hunter