Actively Recruiting

Phase 3
Age: 18Years - 60Years
All Genders
NCT06386783

Fentanyl Versus Dexmedetomidine as an Adjuvant to Bupivacaine in Spinal Anesthesia ; Peritoneal Symptomatic Effects

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

148

Participants Needed

1

Research Sites

86 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To compare whether 5 μg dexmedetomidine with 25 μg fentanyl added to 0.5% hyperbaric bupivacaine as adjuvants in spinal anaesthesia in patients undergoing appendectomy could reduce intraoperative peritoneal related symptoms.

CONDITIONS

Official Title

Fentanyl Versus Dexmedetomidine as an Adjuvant to Bupivacaine in Spinal Anesthesia ; Peritoneal Symptomatic Effects

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • ASA physical status class I and II
  • Age between 18 and 60 years
  • Either sex
Not Eligible

You will not qualify if you...

  • ASA physical status class III and IV
  • Infection at the site of injection
  • Coagulopathy or use of anticoagulants
  • Congenital anomalies of the lower spine
  • Active disease of the central nervous system
  • Allergy to local anesthetics or the adjuvants
  • Complicated appendicitis

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, 81528

Actively Recruiting

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Research Team

S

Soudy S Hammad, MD

CONTACT

A

Ahmed M Hagag, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Fentanyl Versus Dexmedetomidine as an Adjuvant to Bupivacaine in Spinal Anesthesia ; Peritoneal Symptomatic Effects | DecenTrialz