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NCT02678585 Clinical Trial

Nalbuphine as an Adjuvant to Intravenous Regional Anesthesia

Postoperative Pain Clinical Trial

Official title:
Nalbuphine as an Adjuvant to Intravenous Regional Anesthesia

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02678585
Other study ID # 000087161
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 2015
Est. completion date March 2016

Study information
Verified date June 2018
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The effect of addition of nalbuphine to lidocaine in intravenous regional anesthesia

Recruitment information / eligibility
Status Completed
Enrollment 106
Est. completion date March 2016
Est. primary completion date March 2016
Accepts healthy volunteers No
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

- adult patients

- American Society of Anesthesiologists (ASA) physical status I-II

- age between 20 and 50 years old

- scheduled for elective unilateral short hand surgery

Exclusion Criteria:

- allergy to study medications

- body mass index > 35 kg/m2

- patients with sickle cell disease or Reynaud disease

- patient refusal

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Nalbuphine
53 patients received intravenous regional lidocaine plus nalbuphine
• Lidocaine
53 patients received intravenous regional lidocaine

Locations
Country Name City State
Egypt Assiut university hospital Assiut

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Tourniquet and postoperative pain measured by visual analogue scale 4 hours
Secondary Cortisol level 4 hours
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