Actively Recruiting

Phase 3
Age: 18Years - 70Years
All Genders
NCT06386770

Systemic Versus Local Dexmedetomidine as An Adjuvant to Bupivacaine in Ultrasound Guided Erector Spinae Block

Led by Aswan University · Updated on 2025-02-21

75

Participants Needed

1

Research Sites

39 weeks

Total Duration

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AI-Summary

What this Trial Is About

The aim of this study is to investigate the analgesic effect of local versus systemic dexamedetomedine as adjuvant to bupivacaine in erector spinae block in kidney exploration surgeries.

CONDITIONS

Official Title

Systemic Versus Local Dexmedetomidine as An Adjuvant to Bupivacaine in Ultrasound Guided Erector Spinae Block

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing kidney exploration surgeries
  • ASA physical status I or II
  • Body mass index (BMI) less than 35
Not Eligible

You will not qualify if you...

  • Use of opioid analgesics before surgery
  • Local infections at the injection site for the block
  • ASA physical status III or IV
  • Pregnancy
  • History of drug addiction, alcohol abuse, or psychiatric illness

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Aswan University

Aswān, Aswan Governorate, Egypt, 81511

Actively Recruiting

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Research Team

T

Tarek s Hemaida, MD

CONTACT

S

Soudy s Hammad, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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