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TED Stocking vs. Reparel Garment After Hip Replacement

R

Reparel

Status

Active, not recruiting

Conditions

Osteoarthritis (OA) of the Hip

Treatments

Device: TED Stocking
Device: Reparel Bioactive Sleeve

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

This randomized, prospective study compares the effectiveness of a novel bioactive garment (Reparel Leg Sleeve) versus standard TED compression stockings in reducing postoperative leg swelling, pain, and deep vein thrombosis (DVT) rates following total hip arthroplasty. The study aims to determine whether the bioactive garment improves patient comfort and recovery outcomes compared to traditional stockings.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 89 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-89
  • Undergoing primary unilateral total hip replacement
  • BMI < 40
  • Able to follow postoperative protocol
  • English speaking

Exclusion criteria

  • Age <18 or >90
  • Physical inability to use stockings
  • Allergy to silicone/polyester
  • Active DVT
  • History of vascular bypass on operative limb (e.g., Fem-Pop, Fem-Fem)
  • Inability to comply with post-op/rehab
  • Lymphedema

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

Bioactive Sleeve on Operative Leg
Experimental group
Description:
Participants receive the Reparel Bioactive Sleeve on the operative leg and the Standard TED Stocking on the non-operative leg.
Treatment:
Device: Reparel Bioactive Sleeve
Bioactive Sleeve on Non-Operative Leg
Active Comparator group
Description:
Participants receive the Reparel Bioactive Sleeve on the non-operative leg and the Standard TED Stocking on the operative leg.
Treatment:
Device: TED Stocking

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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