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NCT03150732 Clinical Trial

Systemic Nalbuphine Versus Intravenous Regional Anesthesia

Postoperative Pain Clinical Trial

Official title:
Comparison of Systemic Nalbuphine Versus Intravenous Regional Anesthesia

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03150732
Other study ID # 000087273
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 10, 2022
Est. completion date February 10, 2024

Study information
Verified date February 2024
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparison of systemic nalbuphine versus intravenous regional anesthesia in patients undergoing hand surgery.

Recruitment information / eligibility
Status Completed
Enrollment 82
Est. completion date February 10, 2024
Est. primary completion date February 10, 2024
Accepts healthy volunteers No
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria: - Patients scheduled for elective unilateral hand surgery. Exclusion Criteria: - Patient refusal. - Allergy to study medications - Body mass index > 35 kg/ m2 - Patients with sickle cell or Reynaud diseases - Patients with a history of psychiatric illness or on chronic opioids

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Systemic nalbuphine
Patients will receive systemic nalbuphine 10 mg
• Local nalbuphine
Patients will receive local nalbuphine 10 mg

Locations
Country Name City State
Egypt Mohamed H Bakri Assiut

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Duration of postoperative Analgesia minutes Postoperative 24 hours
Secondary Diclofenac analgesic consumption mg Postoperative 24 hours
Secondary Cortisol level Level of cortisone in blood (nmol/L) Preoperative and at 4 hours after skin incision
Secondary Severity of postoperative Pain Visual Analogue Scale (VAS) Postoperative 24 hours
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