Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06826690

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

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

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Aswan university hospital

Aswān, Aswan Governorate, Egypt

Location status: Recruiting

About this study

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

Taking medical and surgical history from patients. Taking base line data as heart rate and blood pressure and spo2. Measure duration of analgesia for post operative pain using NRS for 24 hours abd recording NRS at time interval of 2 , 4,6,12,24 hours post operative.

Any patient the NRS above 4 will receive 5 mg nalbufin . Recording patients satisfaction by a survey .

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients more than or equal 18 years old and are ASA 1-3

Exclusion criteria

  • allergy to used medication
  • pre exist neuropathy
  • coagulapthy
  • cognitive impairment
  • refusal to participate
  • Failed block and requiring general anesthesia

Treatment and study plan

Group 1: ultrasound guided wrist block with bupivacane alone

Procedure

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

Group 2 : ultrasound guided wrist block with bupivacane and dexamethasone

Procedure

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

Group 3: ultrasound guided wrist block with bupivacane and dexametmiodine

Procedure

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

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

Procedure

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

Primary outcomes

  1. Comparing the effectiveness of bupivacane alone and bupivacane with dexamethasone and bupivacane with dexametmiodine and bupivacane with dexamethasone and dexametmiodine

    Time frame: 24 hour

    Comparing duration of analgesia by each combination from block administration to first request of analgesia

Study contacts

Contact information is provided by the study sponsor or research team.

Mahmoud RAFAAT Mohamed, Resident doctor

CONTACT

[email protected]

201024289235

Sponsors and collaborators

Lead sponsor

Mahmoud Rafaat Mohamed

Other

Registry information

Official study title

A Comparative Factorial Study Design of Adjuvant Enhanced Ultrasound-Guided Wrist Block Anaesthesia for Hand Surgery : Bupivacane, Dexamethasone, Dexametmiodine

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Feb 14, 2025
Registry last updated
Mar 26, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.