Clinical Trials Logo

Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00348907
Other study ID # DCIC 05 45
Secondary ID
Status Terminated
Phase Phase 3
First received July 4, 2006
Last updated October 31, 2007
Start date July 2006
Est. completion date December 2006

Study information

Verified date October 2007
Source Association Francaise pour la Recherche Thermale
Contact n/a
Is FDA regulated No
Health authority France: Ministry of Health
Study type Interventional

Clinical Trial Summary

The main objective of this study is to demonstrate that hydrotherapy in a specific place can reduce the risk of post-thrombotic syndrome.


Description:

Venous thrombo-embolic disease (VTED) is a frequent pathology. The incidence is about 5 to 20 cases for 10000 persons each year, in a general population. The immediate risk is the pulmonary embolism potentially fatal. So, it justifies all the works in clinical research during the last years. Those studies allow many progresses, diagnostic and therapeutic, for the immediate undertaking of the patients. Despite that, VTED is a major problem of public health and the diminution of the mortality lied to VTED is one of the objectives of the French law relative to the politics of Public Health (August 2004). At more long-term, the post-thrombotic syndrome lead to an incapacitating pathology, which requires many cares. The frequency of the post-thrombotic syndrome is evaluated between 25 and 60% at middle-term (1 or 2 years). It depends of the studies and of the clinical primary end-points or vascular explorations. Rehabilitation has never been validated in this indication by studies with a correct methodology.

Deep venous thrombosis (not in acute phase) is recognized as an indication for about 10 spa in France. But the specific or global benefit of this water cure is not clearly and scientifically proved. The importance of the venous pump of the calf and of the hydrostatic pressure in the physiopathology of the post-thrombotic syndrome make natural the use of balneotherapy for the prevention of this pathology for patients with severe deep venous thrombosis of lower limbs (proximal and obstruent). The venous thermal techniques have well-defined physiopathological targets. The haemodynamic and microcirculatory effects of some of them have been proved. The high degree of satisfaction of the patients that benefit from phlebological water cure every year in France indirectly shows the benefits that they feel. In those indications, prevention of the post-thrombotic syndrome is one of the well-recognize by the medical profession. For all that, there was not really validation of this indication with an acceptable methodology for the canons of the modern medicine. That is the reason why we undertake this randomized, single-blind controlled study with for main objective to demonstrate that hydrotherapy in a specific place can reduce the risk of post-thrombotic syndrome.


Recruitment information / eligibility

Status Terminated
Enrollment 3
Est. completion date December 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- both sexes;

- 18 years old and more;

- clinical indication of thermal cure (first phase of deep venous thrombosis authenticated by unilateral venous echo-doppler

- curative anticoagulant treatment more than 3 month;

- oedema and/or spontaneous pain with functional discomfort;

- available for a thermal cure during 18 days and a follow-up period of 36 month;

- voluntary to participate to the study, informed consent form signed after appropriate information;

- affiliation to the social security system or equivalent;

- no previous participation to a thermal cure (in the indication of phlebology)

Exclusion Criteria:

- isolate distal thrombosis;

- asymptomatic thrombosis;

- cutaneous ulcer of lower limb;

- refusal to consent;

- refusal to benefit of thermal cure;

- contra-indication to hydrotherapy.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
thermal cure
thermal cure of 18 days including movement in swimming pool, mud-bath, shower, massage and thermal steam
late thermal cure
thermal cure of 18 days including movement in swimming pool, mud-bath, shower, massage and thermal steam at 2 years

Locations

Country Name City State
France Etablissement thermal Argeles-Gazost
France Etablissement thermal Bagnoles de l'orne
France Etablissement thermal Barbotan-les-thermes
France Bérot Dax
France Borda Dax
France Dax thermal Dax
France Foch Dax
France L'avenue DAX
France Le Grand Hôtel Dax
France Le miradour Dax
France Le Regina Dax
France Le Splendid Dax
France Les arènes DAX
France Les écureuils Dax
France Les thermes Dax
France Saint-Pierre Dax
France Sarrailh Dax
France Etablissement thermal Evian-les-bains
France Domaine d'heurteboise Jonzac
France Etablissement thermal La Léchère
France Etablissement thermal Luxeuil-les-bains
France Etablissement thermal Luz-saint-sauveur
France Etablissement thermal Rochefort-sur-mer
France Caliceo Saint-Paul-les-Dax
France Chênes Saint-Paul-les-Dax
France Christus Saint-Paul-les-Dax
France Etablissmeent thermal Saubusse-les-bains

Sponsors (1)

Lead Sponsor Collaborator
Association Francaise pour la Recherche Thermale

Country where clinical trial is conducted

France, 

References & Publications (5)

Asbeutah AM, Riha AZ, Cameron JD, McGrath BP. Reproducibility of duplex ultrasonography and air plethysmography used for the evaluation of chronic venous insufficiency. J Ultrasound Med. 2005 Apr;24(4):475-82. — View Citation

Kahn SR, Kearon C, Julian JA, Mackinnon B, Kovacs MJ, Wells P, Crowther MA, Anderson DR, Van Nguyen P, Demers C, Solymoss S, Kassis J, Geerts W, Rodger M, Hambleton J, Ginsberg JS; Extended Low-intensity Anticoagulation for Thrombo-embolism (ELATE) Investigators. Predictors of the post-thrombotic syndrome during long-term treatment of proximal deep vein thrombosis. J Thromb Haemost. 2005 Apr;3(4):718-23. Epub 2005 Feb 23. — View Citation

Labropoulos N, Leon LR Jr. Duplex evaluation of venous insufficiency. Semin Vasc Surg. 2005 Mar;18(1):5-9. Review. — View Citation

Launois R, Reboul-Marty J, Henry B. Construction and validation of a quality of life questionnaire in chronic lower limb venous insufficiency (CIVIQ). Qual Life Res. 1996 Dec;5(6):539-54. — View Citation

Prandoni P, Lensing AW, Cogo A, Cuppini S, Villalta S, Carta M, Cattelan AM, Polistena P, Bernardi E, Prins MH. The long-term clinical course of acute deep venous thrombosis. Ann Intern Med. 1996 Jul 1;125(1):1-7. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Presence at 1 year of a severe post-thrombotic syndrome clinically defined. 1 year
Secondary Post-thrombotic syndrome at 2 years; 2 years
Secondary Quality of life: CIVIQ Scale; inclusion, 1, 2 years before and after thermal cure
Secondary Intensity of the symptoms of venous insufficiency auto evaluation by patient monthly
Secondary Deep venous reflux (evaluated by echo-doppler); inclusion, 1 and 2 years
Secondary Persistence of a residual thrombus (echo-doppler); inclusion, 1 and 2 years
Secondary Correlation between clinical evolution and echo-doppler evolution of the venous after-effects; 1 year
Secondary Benefit of a late cure at 2 years. 2 years
See also
  Status Clinical Trial Phase
Active, not recruiting NCT05559255 - Changes in Pain, Spasticity, and Quality of Life After Use of Counterstrain Treatment in Individuals With SCI N/A
Terminated NCT04356352 - Lidocaine, Esmolol, or Placebo to Relieve IV Propofol Pain Phase 2/Phase 3
Completed NCT04748367 - Leveraging on Immersive Virtual Reality to Reduce Pain and Anxiety in Children During Immunization in Primary Care N/A
Completed NCT05057988 - Virtual Empowered Relief for Chronic Pain N/A
Completed NCT04466111 - Observational, Post Market Study in Treating Chronic Upper Extremity Limb Pain
Recruiting NCT06206252 - Can Medical Cannabis Affect Opioid Use?
Recruiting NCT05868122 - A Study to Evaluate a Fixed Combination of Acetaminophen/Naproxen Sodium in Acute Postoperative Pain Following Bunionectomy Phase 3
Active, not recruiting NCT05006976 - A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study N/A
Completed NCT03273114 - Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain N/A
Enrolling by invitation NCT06087432 - Is PNF Application Effective on Temporomandibular Dysfunction N/A
Completed NCT05508594 - Efficacy and Pharmacokinetic-Pharmacodynamic Relationship of Intranasally Administered Sufentanil, Ketamine, and CT001 Phase 2/Phase 3
Recruiting NCT03646955 - Partial Breast Versus no Irradiation for Women With Early Breast Cancer N/A
Active, not recruiting NCT03472300 - Prevalence of Self-disclosed Knee Trouble and Use of Treatments Among Elderly Individuals
Completed NCT03678168 - A Comparison Between Conventional Throat Packs and Pharyngeal Placement of Tampons in Rhinology Surgeries N/A
Completed NCT03931772 - Online Automated Self-Hypnosis Program N/A
Completed NCT03286543 - Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty Using the SPRINT Beta System N/A
Completed NCT02913027 - Can We Improve the Comfort of Pelvic Exams? N/A
Terminated NCT02181387 - Acetaminophen Use in Labor - Does Use of Acetaminophen Reduce Neuraxial Analgesic Drug Requirement During Labor? Phase 4
Recruiting NCT06032559 - Implementation and Effectiveness of Mindfulness Oriented Recovery Enhancement as an Adjunct to Methadone Treatment Phase 3
Active, not recruiting NCT03613155 - Assessment of Anxiety in Patients Treated by SMUR Toulouse and Receiving MEOPA as Part of Their Care