Hemorrhoids Clinical Trial
— RADOOfficial title:
Prospective, Multicentric, Randomized, Open-label Study Comparing the Efficacy, in Terms of Quality of Life, and Safety of RAdiofrequency Versus HAL- RAR DOppler in Hemorrhoidal Pathology
NCT number | NCT04896268 |
Other study ID # | RADO study |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | January 3, 2023 |
Est. completion date | August 2025 |
Haemorrhoids are composed of tissue rich in blood vessels and are present in all individuals inside the anus (internal haemorrhoids) or under the skin of the anus (external haemorrhoids). Haemorrhoidal disease (HD) occurs when haemorrhoids become troublesome and cause symptoms such as pain, bleeding, prolapse or oozing. In case of failure of medical treatment, instrumental procedures or extensive disease, surgical treatment can be considered. There are two classic surgical techniques. The first is the pedicle haemorrhoidectomy of the Milligan and Morgan type. The second classic surgical technique is the Longo stapled anopexy. Recently, less invasive surgical techniques such as arterial ligation (HAL, with or without Doppler) followed by recto-anal repair (RAR for "Recto Anal Repair") and sometimes associated with mucopexy, which allows the excess mucosa to be ligated and the muco-haemorrhoidal tissue to be fixed to the rectal wall, have developed. The use of radiofrequency current (Rafaelo technique) in the treatment of haemorrhoidal disease is an innovative technique of haemorrhoidal thermocoagulation. It is a mini-invasive technique, which can be performed under sedation or short general anaesthesia (GA), with little pain, allowing a rapid return to normal life and a short time off work. Although this technique is already used in other European countries: Poland, Germany, Belgium, Great Britain (UK), there is now a Polish, German, Spanish and English study in the process of publication. There have been no studies in France to evaluate this new technique and assess its good tolerance, the duration of work stoppage, the improvement in quality of life and the evaluation of its effectiveness.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | August 2025 |
Est. primary completion date | January 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: - Male or Female consulting for hemorrhoidal pathology (grade II or III) after failure of medico-instrumental treatments. - Age = 18 years and < 75 years - Mandatory affiliation to a health insurance system. - Patient having been informed of the study and having given informed consent Exclusion Criteria: - Patients with chronic inflammatory bowel disease - Patients with suspected gastro-colic pathology - Haematological diseases - Anal fistulas - Patients unable to discontinue anti-vitamin K or oral anticoagulants - Associated anal fissure - External haemorrhoidal disease - Pregnant or breastfeeding women - Patients under legal protection |
Country | Name | City | State |
---|---|---|---|
France | Private hospital Guillaume de Varye | Saint-Doulchard | |
France | Centre Clinical | Soyaux |
Lead Sponsor | Collaborator |
---|---|
Elsan |
France,
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Becq A, Camus M, Rahmi G, de Parades V, Marteau P, Dray X. Emerging indications of endoscopic radiofrequency ablation. United European Gastroenterol J. 2015 Aug;3(4):313-24. doi: 10.1177/2050640615571159. — View Citation
BORD C., PILLANT H., FAVREAU-WELTZER C., SENEJOUX A., SOUDAN D., ARREDONDO BISONO T., ZKIK A., BERDEAU G., ABRAMOWITZ L. Development of A Validated Questionnaire Evaluating The Burden of The Haemorrhoidal Disease and Anal Fissure (Hemo-Fiss). Value in Health, VOLUME 18, ISSUE 7, PA630, NOVEMBER 01, 2015
Brown SR, Tiernan JP, Watson AJM, Biggs K, Shephard N, Wailoo AJ, Bradburn M, Alshreef A, Hind D; HubBLe Study team. Haemorrhoidal artery ligation versus rubber band ligation for the management of symptomatic second-degree and third-degree haemorrhoids (HubBLe): a multicentre, open-label, randomised controlled trial. Lancet. 2016 Jul 23;388(10042):356-364. doi: 10.1016/S0140-6736(16)30584-0. Epub 2016 May 25. Erratum In: Lancet. 2016 Jul 23;388(10042):342. — View Citation
CRETON D. et le groupe closure®.Oblitération tronculaire saphène par le procédé radiofréquence VNUS Closure ®. résultats à 5 ans de l'étude multicentrique prospective,Phlébologie 2006,59 :67-72
Loder PB, Kamm MA, Nicholls RJ, Phillips RK. Haemorrhoids: pathology, pathophysiology and aetiology. Br J Surg. 1994 Jul;81(7):946-54. doi: 10.1002/bjs.1800810707. — View Citation
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Pigot F, Siproudhis L, Allaert FA. Risk factors associated with hemorrhoidal symptoms in specialized consultation. Gastroenterol Clin Biol. 2005 Dec;29(12):1270-4. doi: 10.1016/s0399-8320(05)82220-1. — View Citation
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VIVALDI.C,. TOLKSDORFS. SCHAFER H., Radiofrequency ablation of hemorroïds. First results of a new technique The Rafaelo Procedure.Endarmpraxis;Colorectal disease 2017, 19 (suppl 2) p.138
* Note: There are 11 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To demonstrate an increase in quality of life, at 1 month post-procedure, when haemorrhoidal disease is managed with radiofrequency versus HAL-RAR with Doppler | The Haemorrhoidal Disease and Anal Fissure questionnaire | 1-month visit | |
Secondary | Pain evaluation | Numerical scale (minimum: 0; maximum: 10) | 1-month visit | |
Secondary | Pain evaluation | Numerical scale (minimum: 0; maximum: 10) | 6-month visit | |
Secondary | feasibility of the 2 techniques under simple antiplatelet agents, anti-vitamin K or oral anticoagulant. | Success rate of radiofrequency procedure to be compared between patients taking or not taking AAP, AOD or VKA | 6-month visit | |
Secondary | Occurrence of a relapse | date of relapse, if relapse | through study completion, an average of 6 months | |
Secondary | Recording of specific symptoms that indicate improvement in hemorrhoidal disease | Occurrence of bleeding / prolapse | through study completion, an average of 6 months | |
Secondary | Time to return to work | Duration of work interruption (in days) | through study completion, an average of 6 months | |
Secondary | Safety evaluation | Adverse event | through study completion, an average of 6 months |
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