Arthroscopic Partial Meniscectomy Time Window

NCT ID: NCT05655442

Last Updated: 2023-03-14

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

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Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2020-01-12

Study Completion Date

2023-08-28

Brief Summary

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The purpose was to assess knee function outcomes between early arthroscopic partial meniscectomy(APM) and delayed APM for patients with degenerative meniscus lesions(DMLs)

Detailed Description

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Whether early APM surgery or delayed APM surgery will more benefit for patients with DMLs. The study was to determine the early APM vs delayed APM effect on knee function outcomes for patients with DMLs for 1 year follow-up.

Conditions

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Meniscus Lesion

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

Study Groups

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early APM

early APM within 3 and 6 month knee pain symptoms

Group Type EXPERIMENTAL

early APM

Intervention Type PROCEDURE

early APM within 3 and 6 month knee pain symptoms

delayed APM

delayed APM within 6 and 12 month knee pain symptoms

Group Type ACTIVE_COMPARATOR

delayed APM

Intervention Type PROCEDURE

delayed APM within 6 and 12 month knee pain symptoms

Interventions

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early APM

early APM within 3 and 6 month knee pain symptoms

Intervention Type PROCEDURE

delayed APM

delayed APM within 6 and 12 month knee pain symptoms

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* • Clinical diagnosis of degenerative meniscus lesions based on knee MRI

Exclusion Criteria

* • Must be able to have no acute knee injury such as car crash or acute sports injury;

* Must be able to have no knee surgeries history;
* Must be able to have no rheumatoid arthritis or serious knee osteoarthritis with deformity;
* Must be able to have no contraindications to MRI;
* Must be able to have no severe cardiopulmonary disease;
* Must be able to have no musculoskeletal or neuromuscular impairments ;
* Must be able to have good visual, hearing, or cognitive;
Minimum Eligible Age

35 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shenzhen People's Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Hongyu Wang, Doctor

Role: PRINCIPAL_INVESTIGATOR

Shenzhen People's Hospital

Other Identifiers

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SZlesions

Identifier Type: -

Identifier Source: org_study_id

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