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NCT03875274 Clinical Trial

Morphine Added to Ropivacaine for FICB for Postoperative Analgesia

Postoperative Pain Clinical Trial

Official title:
Postoperative Analgesic Effect of Morphine Added to Ropivacaine for Fascia Iliaca Compartment Block Following Femoral Fracture Surgeries

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03875274
Other study ID # IRC/0832/016
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date April 1, 2017
Est. completion date December 31, 2017

Study information
Verified date June 2022
Source B.P. Koirala Institute of Health Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

prospective, randomized double blinded study to investigate the effects of morphine as an adjuvant to ropivacaine on FICB

Recruitment information / eligibility
Status Completed
Enrollment 70
Est. completion date December 31, 2017
Est. primary completion date December 31, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - All patients undergoing elective femur surgery under spinal anaesthesia - Age group (18-65 years) - ASA physical status I and II Exclusion Criteria: - • Not willing to participate in the study - Other painful co-morbidities (neuropathies) - Allergy or any contraindication to study medication - Psychiatric disorder - Coagulopathy - Infection at the site of the block - Use of other modes of anaesthesia or analgesia besides spinal anaesthesia.

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Ropivacaine, Morphine
Morphine added to ropivacaine for fascia iliaca compartment block
• Ropivacaine, Saline
Normal saline added to ropivacaine for fascia iliaca compartment block

Locations
Country Name City State
Nepal BPKIHS Dharan Bazar Sunsari

Sponsors (1)
Lead Sponsor Collaborator
B.P. Koirala Institute of Health Sciences

Country where clinical trial is conducted

Nepal, 

Outcome
Type Measure Description Time frame Safety issue
Primary Duration of Analgesia The period in minutes when the patient is free of pain 24 hours
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