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Comparative Factorial Study Design of Ultrasound Guided Wrist Block for Hand Surgery Comparing Effect of Bupivacane Alone and Bupivacane with Dexamethasone and Bupivacane with Dexametmiodine and Bupivacane with Dexamethasone and Dexametmiodine

NCT06826690 · Status: RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 160

Last updated 2025-03-26

No results posted yet for this study

Summary

Ultrasound guided wrist block comparing effect of bupivacane alone and bupivacane with dexamethasone and bupivacane with dexametmiodine and bupivacane with dexamethasone and dexametmiodine

Conditions

  • Hand Surgeries

Interventions

PROCEDURE

Group 1: ultrasound guided wrist block with bupivacane alone

Ultrasound guided wrist block with 15 ml volume of bupivacane.25%

PROCEDURE

Group 2 : ultrasound guided wrist block with bupivacane and dexamethasone

Group 2 : patients receive ultrasound guided wrist block with bupivacane.25% and 8 mg dexamethasone.. 15 ml volume totally

PROCEDURE

Group 3: ultrasound guided wrist block with bupivacane and dexametmiodine

Group 3 will receive ultrasound guided wrist block with bupivacane.25% and 50 mcg dexametmiodine... 15 ml volume totally

PROCEDURE

Group 4: patients will receive ultrasound guided wrist block with bupivacane and dexamethasone and dexametmiodine

Group 4 patients will receive ultrasound guided wrist block with bupivacan.25%e and 8 mg dexamethasone and 50 mcg dexametmiodine

Sponsors & Collaborators

  • Mahmoud Rafaat Mohamed

    lead OTHER

Principal Investigators

  • Zaher Zaki Zaher, Specialist

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-02-02
Primary Completion
2025-08-07
Completion
2025-09-10
FDA Drug
Yes
FDA Device
Yes

Countries

  • Egypt

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06826690 on ClinicalTrials.gov