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CompletedNCT07637344TGLPRUpdated Jun 9, 2026

Tactile Guided Lateral Patellar Release

An interventional study of Percutaneous lateral retinacular release of the patella in Lateral Patellar Compression Syndrome, Patellar Dislocation and Patellar (or Kneecap) Instability and Mal-alignment, sponsored by Issa, Abdulhamid Sayed, M.D.. Completed. Open to participants aged 16 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-06-09.

Sponsored by Issa, Abdulhamid Sayed, M.D. · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 11 years 10 months after the study started (first participant enrolled Jul 2014, registered May 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
23
Allocation
Not applicable
Ages
16 Years to 65 Years
Sex
All
01

Study summary

The lateral edge of the patella is identified by the surgeon's finger and the lateral ligament incision is performed with a blade through the skin.

Read the detailed description

Under short-acting general anesthesia, the patient lies supine. The surgeon palpates to identify the lateral border of the patella; typically, the surgeon's left thumb is placed at the midpoint of this lateral edge. Using a No. 11 scalpel blade, an incision is made parallel to the lateral border of the patella-approximately 5 mm away-extending through the skin, subcutaneous layers, and lateral retinaculum, and penetrating the knee's synovial membrane to enter the joint space. This creates a small "keyhole" opening suitable for knee arthroscopy, with the sharp edge of the blade initially oriented toward the patient's head.

The tip of the blade is then angled inward into the joint to incise the lateral retinaculum superiorly, without enlarging the initial skin puncture.

The blade is then rotated 180 degrees so that its sharp edge faces toward the patient's feet. The inferior portion is incised by angling the blade inward through the subcutaneous layers, lateral retinaculum, and synovial membrane into the joint, while maintaining the original shape and size of the skin puncture without enlargement.

A sterile dressing and a compression bandage are then applied, and the patient is encouraged to begin early mobilization.

3. Comparison of Clinical Success Rates Surgical Goal Isolated Release Release + Realignment Stability Success \~77.3% \~93.6% Recurrence Rate Higher (odds \~0.29) Lower (odds \~0.06)

02

Conditions studied

  • Lateral Patellar Compression Syndrome
  • Patellar Dislocation
  • Patellar (or Kneecap) Instability and Mal-alignment
  • Patella Alta
  • Patella Chondromalacia
  • Patella Dislocation Recurrent
  • Patella Dysplasia
  • Patella Subluxation
  • Patellar Femoral Syndrome
  • Patellar Crepitus
  • Patella Position

Keywords

  • Tactile Guided Lateral Patellar Release
  • TGLPR
  • Pie Crust
  • Capsule-Uncut Immaculate
  • CUI
  • Lateral Retinacular Lengthening
  • Z-Plasty
  • Open Lateral Release
  • Isolated LPR
  • LPR
  • Lateral Patellar Compression Syndrome
  • LPCS
  • lateral retinacular release
03

In context

Patellar Dislocation

41 studies on the registry are indexed under Patellar Dislocation; 9 are open to participants now.

This study's enrollment of 23 is below the median of 50 across 22 interventional studies indexed under Patellar Dislocation.

Browse Patellar Dislocation studies →

Lead sponsor

Issa, Abdulhamid Sayed, M.D. is the lead sponsor of 5 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Retropatellar Pain
  • Lateral Patellar Pain

Exclusion criteria

Exclusion Criteria:

  • Knee Arthritis grade 4
  • Totally Knee Arthritis
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
23 participants (actual)

Study arms

  • Experimental
    Tactile Guided Lateral Patellar Release

    Percutaneous lateral retinacular release of the patella

    Procedure: Percutaneous lateral retinacular release of the patella

Interventions

  • ProcedurePercutaneous lateral retinacular release of the patella

    The lateral edge of the patella is identified by the surgeon's finger and the lateral ligament incision is performed with a blade through the skin.

06

What researchers measure

Primary outcomes

  1. Less open surgery trauma

    Directly going to the goal lesion with less expansion

    Time frame: [Time Frame: 3 minutes to 5 minutes,]

07

Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jul 2014 to primary completion in Nov 2025, 136 months.

How these figures are worked out, and which studies are left out of them.

Registered
May 28, 2026
First posted
Jun 9, 2026
StartActual
Jul 1, 2014
Primary completionActual
Nov 30, 2025
CompletionActual
Mar 31, 2026
Last update
Jun 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07637344
Lead sponsor
Issa, Abdulhamid Sayed, M.D.
Responsible party
Sponsor
First posted
Jun 9, 2026
Start date
Jul 1, 2014
Primary completion
Nov 30, 2025
Completion
Mar 31, 2026
Last update
Jun 9, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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