Clinical Trials Logo

Clinical Trial Summary

The restriction of the range of motion is one of the most frequently encountered complications after the surgical procedures of the knee. While the flexion deficit is relatively well tolerated, even the small extension deficit significantly impairs the quality of life due to the increased stress on the patellofemoral joint, functional leg length discrepancy and the subsequent mechanical overload in the hip joint, lumbar spine and contralateral knee. In the majority of cases the guided physiotherapy protocol is sufficient to restore the full range of motion. In refractory cases, the treatment consists of the thorough arthrolysis of the affected knee, aiming to excise the adhesions, osteophytes and orthopaedic implants interfering with the knee range of motion. However, as the extension deficit persists, the contracture of the knee posterior capsule may develop and the sole debridement of the knee may be insufficient. In such rare cases the treatment consists of the posterior capsulotomy of the affected joint. Traditionally, this procedure was performed through the open approach. However, with the growing indications toward the arthroscopic procedures seen in recent decades, even such salvage procedures like posterior knee capsulotomy are increasingly performed through the arthroscopic approach. The aim of this study is to assess the outcomes of the arthroscopic complete posterior capsulotomy of the knee basing on the knee range of motion and functional outcomes. The primary outcome consists of the knee extension, whereas the secondary outcomes include knee flexion, knee total range of motion, The International Knee Documentation Committee Questionnaire and the Knee injury and Osteoarthritis Outcome Score.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05385393
Study type Interventional
Source Artromedical Konrad Malinowski Clinic
Contact Konrad Malinowski, MD PhD
Phone +48 509 812 212
Email malwin8@wp.pl
Status Recruiting
Phase N/A
Start date June 1, 2020
Completion date June 1, 2025

See also
  Status Clinical Trial Phase
Terminated NCT04578951 - Measurement of the Quality of Life in Patients Operated With a Total Knee Prosthesis (TKA) From the FHK® Range.
Recruiting NCT05566561 - Para-sartorial Compartment Block in Knee Surgery N/A
Completed NCT05533970 - Ultrasound-guided H-FICB for Arthroscopic Knee Surgery: What is the Optimal Dose of Dexmedetomidine? N/A
Completed NCT04648072 - How Does the Addition of Adductor Canal Block to Local Infiltration Affect Recovery in Patients Undergoing Total Knee Arthroplasty? A Feasibility Study. N/A
Completed NCT05621161 - ESPB vs FICB for Pain Management Following Total Hip Prosthesis Surgery N/A
Completed NCT04388111 - Intraosseous Morphine in Primary TKA Phase 4
Not yet recruiting NCT06284824 - Comparison of Two Robotic-Assisted Total Knee Arthroplasty Systems N/A
Not yet recruiting NCT05749965 - Results of Unicompartmental Knee Arthroplasties in Patients Beyond Historical Indications (PUCIL)
Not yet recruiting NCT06144099 - Prothrombin Complex Concentrate vs Fresh Frozen Plasma in Goal-directed Bleeding Management in Non-cardiac Surgery Phase 4
Recruiting NCT06305858 - Partial Versus Total Knee Replacement in Bicompartmental Gonarthrosis (Medial and Patellofemoral): Prospective Functional Assessment Study N/A
Active, not recruiting NCT05448742 - Biplanar PSI Slope-reducing MOWHTO With Tibial Tuberosity Serving as Hinge Axis: Cadaveric Study N/A
Not yet recruiting NCT05889286 - F18-MHF: Orthopedic Implants-Associated Infection Detection
Active, not recruiting NCT06087562 - iPACK Block for Total Knee Arthroplasty Phase 4
Recruiting NCT04821154 - Persona Revision Knee System Outcomes
Recruiting NCT04422119 - Standard Dressing Versus Moist Dressing in the Course of the Postoperative Wound in Patients With Knee Prosthesis N/A
Recruiting NCT04321629 - Knee Arthritis Treatment With Autologous Fragmented Adipose Tissue and PRP - Comparison of Two Treatment Methods Phase 2
Active, not recruiting NCT04872855 - Observational Study to Evaluate Clinical Performance and Safety in Total Knee Arthroplasty
Completed NCT05669066 - Meditation and Opioid Consumption in Total Joint Replacement Patients Undergo Primary Total Hip and Knee Replacement N/A
Terminated NCT04650594 - Functional Outcomes of Knee Protheses for Malignant Tumours of Bone N/A
Active, not recruiting NCT04221581 - Study Conducted on Patients Operated With a FHK ASYMETRIQUE to Confirm Security and Performance of the Device