MedTrace Logo

Epidural Low Dose Morphine in Postoperative Pain After Posterior Lumbar Spinal Surgery

NCT02067338 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 19

Last updated 2014-02-20

No results posted yet for this study

Summary

The effect of epidural low-dose morphine-soaked microfibrillar collagen sponge in postoperative pain control after posterior lumbar spinal surgery: a randomized, double-blind, placebo-controlled study

Conditions

  • Morphine

Interventions

DRUG

1 mg morphine soak in epidural oxidized cellulose

During posterior lumbar spinal surgery , patients received 1 mg morphine-soaked in epidural oxidized cellulose.

DRUG

normal saline

During posterior lumbar spinal surgery , patients received NSS -soaked in epidural oxidized cellulose.

Sponsors & Collaborators

  • Mahidol University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-08-31
Primary Completion
2013-12-31
Completion
2014-01-31

Countries

  • Thailand

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02067338 on ClinicalTrials.gov