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Completed

NCT Number: NCT01935414

Geko Neuromuscular Stimulator vs Thromboembolism Deterrent Stockings (TEDS): DVT Prevention Study

This study hypothesises that the geko™ device is more efficient than TEDS in preventing the formation of symptomatic/asymptomatic Deep Vein Thrombosis (DVTs), post-surgery.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

BMI The Harbour Hospital

Poole, Dorset, BH15 2BH, United Kingdom

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 18 years of age and over
  • Free of significant abnormal findings as determined by medical history (specifically an absence of DVT or haematological disorders).
  • Has not used any medications (prescribed or over-the-counter including herbal remedies) judged to be significant by the Principal Investigator during the ten (10) days preceding enrolment.
  • Able to understand the Patient Information Sheet and willing to sign the written Informed Consent Form.
  • Able and willing to follow the protocol requirements.

Exclusion criteria

  • Are requiring hip revision surgery
  • History or signs of previous deep or superficial vein thrombosis/pulmonary embolism.
  • Evidence of asymptomatic DVT by Duplex Ultrasound
  • Peripheral arterial disease (ABPI < 0.8), varicose veins or lower limb ulceration or ischemia.
  • Significant varicose veins, phlebitis or lower limb ulceration or ischemia. CEAP Grade 4-6. See Appendix 2
  • Recent surgery within the last 3 months (such as abdominal, gynaecological, hip or knee replacement).
  • Recent trauma to lower limb.
  • Chronic Obesity (BMI Index >40kg/m2).
  • Pregnancy.
  • Significant history of following diseases I. Cardiovascular: Recent MI (< 6 months) II. Percutaneous Coronary Intervention (PCI) with stent (< 3 months for Bare Metal Stent (BMS) and < 12 months for Drug Eluding Stent (DES) III. Moderate to severe CCF, uncontrolled AF IV. Neurological: Stroke, Hemiplegia/Paraplegia, Myopathies V. Significant dermatological conditions affecting lower limbs resulting in broken or inflamed skin particularly at the site where the device is to be fitted.

VI. Clinically significant haematological conditions i.e. coagulation disorders, sickle cell disease VII. Psychiatric disorders

  • On LMWH/Heparin (Prophylactic/therapeutic doses) or Warfarin or warfarin stopped recently and replaced by LMWH/ Heparin
  • Long term steroid with dermatological changes
  • A pulse rate of less than 40 beats/minute
  • A sitting systolic blood pressure >180 and <100 mmHg and/or a sitting diastolic pressure of >100 mmHg.
  • Any significant illness during the four (4) weeks preceding the hip replacement surgery.
  • Participation in any clinical study during the eight (8) weeks preceding the screening period

Treatment and study plan

geko™ post-surgery for 48hrs then 4hrs/day until discharge.

Device

TEDS post-surgery for 48hrs then 4hrs/day until discharge.

Device

Primary outcomes

  1. Presence of asymptomatic DVT assessed by Duplex Ultrasound

    Time frame: 6 weeks

Sponsors and collaborators

Lead sponsor

Firstkind Ltd

Industry

Registry information

Official study title

A Multicentre Randomised Controlled Trial Comparing the Incidence of Asymptomatic and Symptomatic Deep Vein Thrombosis Between the gekoTM Device and Thromboembolism Deterrent Stockings in Patients Recovering From Total Hip Replacement Surgery

Important dates

Study start
2013
Primary completion
2016
Study completion
2016
First posted
Sep 5, 2013
Registry last updated
Aug 5, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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