Auricular Acupuncture for Pain Relief After Ambulatory Knee Arthroscopy

NCT ID: NCT00233857

Last Updated: 2011-02-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE2/PHASE3

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2003-08-31

Study Completion Date

2004-08-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aim was to investigate whether auricular acupuncture is superior to sham acupuncture in relief of acute postoperative pain and in reduction of analgesics consumption on demand and their side effects in patients after ambulatory knee arthroscopy

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Postoperative Pain

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Acute pain postoperative pain auricular acupuncture

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Auricular acupuncture

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Patients with an American Society of Anesthesiologists physical status of I to II scheduled for ambulatory knee arthroscopy under general anesthesia.
2. Surgery time does not exceed 60 minutes.
3. Patients without previous opioid and/or psychiatric medication.
4. Patients ranged 16-65 years old.
5. Patients able to use Visual Analogue Scale-100 for pain intensity measurement.
6. Patients who have given informed consent.

Exclusion Criteria

1. Pregnant or nursing females.
2. Recidivist alcoholics and/or patients with history of psychiatric disease.
3. Local or systemic infection.
4. Age \< 16 and \> 65 years.
5. Surgery time more than 60 minutes.
6. Inability to use Visual Analogue Scale-100.
7. Patients consumed opioid medication before surgery.
8. Patients with prosthetic or damaged cardiac valves (s. Potential risks)
9. Patients who are unable to understand the consent form.
Minimum Eligible Age

16 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University Medicine Greifswald

OTHER

Sponsor Role lead

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Taras I. Usichenko, Assistant Professor

Role: PRINCIPAL_INVESTIGATOR

Anesthesiology and Intensive Care Medicine Department, Ernst Moritz Arndt University of Greifswald, Germany

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Anesthesiology and Intensive Care Medicine Department, University of Greifswald, Germany

Greifswald, , Germany

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Germany

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

III UV 23/03

Identifier Type: -

Identifier Source: org_study_id