Skip to content

Efficacy of Peroperative Suction Drain Usage in Arthroscopic Knee Surgery

Efficacy of Peroperative Suction Drain Usage in Arthroscopic Knee Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02752581
Enrollment
110
Registered
2016-04-27
Start date
2009-01-31
Completion date
2013-04-30
Last updated
2016-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chondropathy, Knee Effusion, Knee Hemarthrosis

Keywords

suction drain, knee arthroscopy, knee pain

Brief summary

The study was designed to investigate efficacy of suction drains in arthroscopic knee surgery, rather than anterior cruciate ligament (ACL) reconstruction. two groups were randomised, and suction drain was applied to one group, and the other group as the control group without a suction drain.

Detailed description

The groups were compared in terms of patellar shock, knee effusion, knee scoring systems, range of motion, loss of labour, hospitalization time. Also different arthroscopic procedures such as meniscectomy, meniscus repair, synovectomy and microfracture were evaluated in terms of need for a suction drain. The controls was at 1st and 15th day, 6th week and 3rd month.

Interventions

A suction drain is used to remove excess fluid from tissues after surgery.

A suction drain is used to remove excess fluid from tissues after surgery.

Sponsors

Mert Özcan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
16 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients with knee derangement and accepted to enroll to the study

Exclusion criteria

* intraarticular fracture, ACL surgery, arthrotomy, bleeding disorder,

Design outcomes

Primary

MeasureTime frameDescription
Rest Pain3 monthsSeverity of pain was evaluated with Visual Analogue Scale (VAS). VAS is a horizontal line divided into ten equal intervals in which zero represents no pain and 10 represents the worst pain ever felt.
Range of Motion3 monthsRange of motion is measures in terms of angular degrees.
Activity Pain3 monthsSeverity of pain was evaluated with Visual Analogue Scale (VAS). VAS is a horizontal line divided into ten equal intervals in which zero represents no pain and 10 represents the worst pain ever felt.

Secondary

MeasureTime frameDescription
loss of labour time1 monthIt is measured in days. It shows the time from discharge to beginning of work.
hospitalization time1 monthIt is measured in days. It shows the period of hospitalization time, from surgery to discharge.
Lysholm3 monthsLysholm is a scoring system from zero to one hundred. It measures subjective complaints of the patients.
International Knee Documentation Committee Score3 monthsis a scoring system from zero to one hundred. It measures subjective complaints of the patients.

Other

MeasureTime frameDescription
Amount of drainage1 dayThe amount of fluid in suction drain. It is measured with cubic centimetre (cc).
patellar shock1.5 monthsPatellar shock was graded in four scales: Grade 1, some notable fluid, Grade 2, minimally elevated patella, Grade 3, patellar ballottement, and Grade 4, tense knee capsule, unable to compress patella.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026