Clinical Trials Logo
  1. Home
  2. Soft Tissue Injuries
  3. NCT03362216

Clinical Efficacy and Safety of Compound Methyl Salicylate Liniment

Soft Tissue Injuries Clinical Trial

Official title:
Clinical Efficacy and Safety of Compound Methyl Salicylate Liniment in the Treatment of Acute and Chronic Soft Tissue Pain：a Multicenter, Randomized, Positive Controlled Clinical Trial

Clinical Trial Summary

This clinical trial program was established according to the ethical principles of the Helsinki declaration and the GCP guiding principle, and a randomized grouping method was used to evaluate the efficacy and safety of Compound Methyl Salicylate Liniment in the treatment of acute and chronic soft tissue pain with a positive control drug, named Diclofenac Sodium Liniment.

Clinical Trial Description

This study is a randomized, double-blind, parallel controlled multicenter clinical trial for evaluate the efficacy and safety of Compound Methyl Salicylate Liniment in the treatment of acute and chronic soft tissue pain with a positive control drug, named Diclofenac Sodium Liniment. A total of 216 participants with acute or chronic tissue pain participated in this clinical trial. The clinical trial cases were equally allocated to each research center, and each center had 30-35 cases. The proportion of patients with acute soft tissue pain and chronic soft tissue pain was 1:1, and the proportion of the experimental group and the control group was 1:1.The observation index include self pain scale record, tenderness scale and swelling, the evaluation period was 7 days.

The statistical analysis plan is prepared by the unit responsible for the statistics, and is prepared before the formal analysis of the data, and is discussed and identified at the blind audit meeting with the major researchers. Statistical analysis will use SAS8.2 statistical analysis software for data processing, and other statistical analysis plan to make detailed provisions. All the statistical tests were two-sided, and the value of P was less than or equal to 0.05, which would be considered statistically significant. Measurement data use case number, mean, standard deviation, minimum, maximum, median and four sub spacing description, counting data and grade data use case number, percentage description. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03362216
Study type Interventional
Source Peking University People's Hospital
Contact
Status Completed
Phase N/A
Start date April 7, 2009
Completion date June 12, 2009
View Details
See also
  Status Clinical Trial Phase
Completed NCT02744144 - Wound Bacterial Microbiota and Their Antibiotic Resistance N/A
Not yet recruiting NCT03872544 - Short Term Status of Free Dermal Fat Autografts for Complex Craniofacial Wounds
Enrolling by invitation NCT03880188 - Long Term Status of Free Dermal Fat Autografts for Complex Craniofacial Wounds
Completed NCT05254470 - Real-World Experience of Patients Treated for Musculoskeletal Injuries With SAM in Routine Care
Recruiting NCT05171673 - Study of PK and Safety of the LicartTM Topical System in Pediatric and Adult Participants With Minor Soft Tissue Injury Phase 3
Not yet recruiting NCT05448807 - Effectiveness of Phentolamine Mesylate as a Reversing Agent for Local Anesthesia in Children Phase 3
Completed NCT02805751 - Early Controlled Loading on Conservative Treated Achilles Tendon Ruptures N/A
Completed NCT05247333 - Implementation of a Minor Ailment Service in Community Pharmacy Practice N/A
Completed NCT04177537 - Real-World Experience of Athletes Treated With SAM
Not yet recruiting NCT04361773 - Effect of Photobiomodulation on the Treatment of Soft Tissue Traumatic Injuries Phase 1/Phase 2
Recruiting NCT05679284 - A Cross-Sectional Observational Study on Retained Drug Needle Fragments in People Who Use Intravenous Drugs
Completed NCT04908748 - Efficacy and Safety of Esflurbiprofen Hydrogel Patch in the Treatment of Local Acute Pain Phase 2
Completed NCT01767727 - Repair of Multiple Finger Defects Using the Dorsal Homodigital Island Flaps N/A
Enrolling by invitation NCT03363971 - Treatment of Posttraumatic Swelling and Pain With Zhi Kang Capsule Phase 4
Completed NCT05399771 - Radiofrequency Hyperthermia Safety Study N/A
Recruiting NCT03544632 - Acellular Adipose Tissue (AAT) for Soft Tissue Reconstruction Phase 2
Completed NCT05982353 - Gelatin Sponge VS PTFE Membrane for Socket Sealing After Immediate Implant Placement Phase 1
Completed NCT04802473 - Flap Thickness Upon Root Coverage With the Use of Acellular Dermal Matrix N/A
Completed NCT01626235 - AMPED Outcomes Registry of Post-ED Pain Management N/A
Completed NCT03049761 - Water Flosser vs String Floss vs Manual Toothbrush Safety N/A