Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01079299 · ClinicalTrials.gov registry record · NA

Effect of Intermittent Pneumatic Compression on Ulcer Healing in Subjects With Secondary Lymphedema

A NA study, sponsored by Calvary Hospital, Bronx, NY.

Completed
Registry status
NA
Development phase
52
Enrollment target

NCT01079299: Completed NA study, sponsored by Calvary Hospital, Bronx, NY.

NCT01079299 is a NA study that has completed, run by Calvary Hospital, Bronx, NY. The registered enrollment target is 52 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01079299, a NA study, has completed, sponsored by Calvary Hospital, Bronx, NY.

COMPLETED
Registry status
NA
Development phase
52 participants
Enrollment target

Study Summary

This is a randomized, controlled, parallel group, open label, clinical trial to evaluate the effectiveness of intermittent, gradient, pneumatic compression (IPC)on the healing of venous ulcers in subjects diagnosed with chronic secondary lymphedema. Time to complete healing, healing rates, edema, wound pain, granulation tissue, and wound exudate (type and amount) will be compared between the IPC-treated group (IPC plus standard compression)and control (standard compression alone).

Primary Outcome

Median number of days for complete healing in each treatment group

Interventions

  • DEVICE Intermittent, gradient, pneumatic compression device

Trial Details

FieldValue
Enrollment Target 52 participants
Start Date 2007-12
Est. Completion 2010-05
Phase NA
Calvary Hospital, Bronx, NY

5 total trials

What the finished NCT01079299 record still lists

NCT01079299 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 52 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 1 intervention - of which Intermittent, gradient, pneumatic compression device is the first listed.

NCT01079299 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01079299 about?

NCT01079299 is a clinical study titled "Effect of Intermittent Pneumatic Compression on Ulcer Healing in Subjects With Secondary Lymphedema". This is a randomized, controlled, parallel group, open label, clinical trial to evaluate the effectiveness of intermittent, gradient, pneumatic compression (IPC)on the healing of venous ulcers in subjects diagnosed with chronic secondary lymphedema. Time to complete healing, healing rates, edema, wo...

What is the current status of trial NCT01079299?

This trial is currently completed. It is a NA study. The enrollment target is 52 participants. The study started on 2007-12. Estimated completion is 2010-05.

What interventions are being tested in trial NCT01079299?

The interventions under investigation include: Intermittent, gradient, pneumatic compression device (DEVICE).

Who is sponsoring clinical trial NCT01079299?

This trial is sponsored by Calvary Hospital, Bronx, NY, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01079299's enrollment target sits among peer trials

52 1272nd of 2000 higher than 722 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02630121 · 52 participants · Phase 4

    Effect of Oxymetazoline Hydrochloride in Combination With Fluticasone Propionate on the Apnea Hypopnea Index (AHI) in Subject With Persistent Nasal Congestion and Mild Obstructive Sleep Apnea

  • NCT03629171 · 52 participants · Phase 2

    Liposome-encapsulated Daunorubicin-Cytarabine and Venetoclax in Treating Participants With Relapsed, Refractory or Untreated Acute Myeloid Leukemia

  • NCT04128748 · 52 participants · Phase 1

    Liposomal Cytarabine and Daunorubicin (CPX-351) and Quizartinib for the Treatment of Acute Myeloid Leukemia and High Risk Myelodysplastic Syndrome

  • NCT04150497 · 52 participants · Phase 1

    Phase 1/2 Study of UCART22 in Patients With Relapsed or Refractory CD22+ B-cell Acute Lymphoblastic Leukemia (BALLI-01)

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01079299, the US trial registry maintained by the National Library of Medicine. NCT01079299 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.