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NCT04775992 Clinical Trial

Preemptive Analgesia of Gabapentoids in Orthopedic Surgery

Acute Postoperative Pain Clinical Trial

Official title:
Preemptive Analgesia of Gabapentoids After Major Orthopedic Surgery: Systematic Review and Meta Analysis

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04775992
Other study ID # KSU
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 1, 2021
Est. completion date December 1, 2021

Study information
Verified date February 2021
Source King Saud University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To address the preemptive analgesic effect of preoperative gabapentoids versus no gabapentoids in orthopedic surgery

Description:

Computer search for all studies used preoperative gabapentoids versus no gabapentoids in orthopedic surgery during the last 10 years (from 2011 - 2020)

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 1000
Est. completion date December 1, 2021
Est. primary completion date July 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - RCT, during last 10 years, involving orthopedic surgery Exclusion Criteria: - non randomized trials, unavailable study data

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• gabapentoids
Preemptive analgesia

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
King Saud University

Outcome
Type Measure Description Time frame Safety issue
Primary Postoperative pain score on rest Pain score by VAS on rest every hour for the first 24 hours
Primary Postoperative pain during movement Pain score by VAS during movements every hour for the first 24 hours
Secondary Worst pain score Highest pain score during the first 24 hours
Secondary Least pain score Lowest pain score during the first 24 hours
Secondary Time spend in severe pain how many hours the patients complaint of severe pain during the first 24 hours
Secondary Patient's satisfaction Satisfaction by the quality of analgesia during the first 24 hours
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