MedTrace Logo

Homeopathy Assessment in Terms of the Consumption of Analgesics After Knee Ligamentoplasty

NCT00222365 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 165

Last updated 2006-11-14

No results posted yet for this study

Summary

This is an add-on, double blind, and randomised clinical trial with three groups: a homeopathic group, a placebo group, and a temporal control group.

The aim of this trial is to assess the effect of homeopathy on the consumption of morphine delivered by PCA (patient control analgesia) for 24 hours after a knee ligamentoplasty.

Conditions

Interventions

DRUG

Arnica montana, 5 CH

DRUG

Bryonia alba, 5 CH

DRUG

Hypericum perforatum, 5 CH

DRUG

Ruta graveolens, 3 DH

Sponsors & Collaborators

  • University Hospital, Grenoble

    lead OTHER

Principal Investigators

  • CRACOWSKI Jean-Luc, Dr · Clinical Trial Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-12-31
Completion
2006-05-31

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

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 NCT00222365 on ClinicalTrials.gov