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Intra-articular Hyaluronan Substitution in Arthroscopy of the Wrist | Clinical Trials | Clareo Health

COMPLETEDNA

Intra-articular Hyaluronan Substitution in Arthroscopy of the Wrist

NCT01254682•TRB Chemedica AG

Summary

The primary objective of this study is to evaluate the efficacy and safety of Ostenil application (1% hyaluronan) after arthroscopy of the wrist.

Eligibility

Age

18 - 80 years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•Male and female patients between 18 and 80 years of age
•Minimum pain score of 2 according to modified Mayo Wrist Score
•Patients in good general health/nutritional condition
•Signed written informed consent

Exclusion Criteria

•Alcohol / drug abuse, drug addiction or neurotic personality disorder; patients with mental illness or suicidal tendency
•Severe intercurrent illness (like uncontrolled diabetes mellitus or thyroid disease, carcinoma,...)
•Fertile women without medically secured contraception(hysterectomy, sterilization, contraceptives,...)
•Subjects having a high probability of non compliance to the study procedures according to investigator's judgement (like illiteracy, insufficient German linguistic knowledge)
•Contraindication for the use of one of the investigational products or for the scheduled anesthesia
•Concomitant or previous participation in a clinical trial within the last 3 months
•Intraarticular treatment with a sodium hyaluronate-based product within the last 6 months
•Intraarticular treatment by the use of corticoid containing substance within the last 3 months
•Concomitant illness or injury influencing study evaluation

Locations (1)

Orthopädische Gemeinschaftspraxis

Straubing, Bavaria, Germany

Key Dates

Start Date

January 1, 2007

Primary Completion Date

August 1, 2009

Completion Date

August 1, 2009

Last Updated

September 28, 2011

Enrollment

140

ACTUAL participants

Conditions

Arthroscopic Surgery

Interventions

Ostenil

DEVICE

Standard arthroscopic procedure

PROCEDURE

Functional Outcomes After Hyaluronic Acid Injections Following Arthroscopy

NCT07468045

Arthroscopic Surgery

View study

NOT_YET_RECRUITINGNA

TIPS Block vs. IV Analgesia for Postoperative Pain After Knee Arthroscopy

NCT07046390

Knee Arthroscopic SurgeryNerve Block

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COMPLETEDPHASE4

Respiratory Impact of LA Volume After IS Block

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: September 28, 2011Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions

Intra-articular Hyaluronan Substitution in Arthroscopy of the Wrist

Inclusion Criteria

Exclusion Criteria

Functional Outcomes After Hyaluronic Acid Injections Following Arthroscopy

TIPS Block vs. IV Analgesia for Postoperative Pain After Knee Arthroscopy

Respiratory Impact of LA Volume After IS Block

Functional Outcomes Following Ankle Fracture Fixation With or Without Ankle Arthroscopy

Analgesic Effect Of Intra-articular Bupivacaine Fentanyl for Postoperative Pain Relief in Knee Arthroscopic Surgery

The Effect of the Shoulder Arthroscopic Surgery on Respiratory Mechanics