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Hemorrhoids clinical trials

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NCT ID: NCT05089500 Not yet recruiting - Hemorrhoids Clinical Trials

The Two Treatment Methods Compared the Sclerosing Agent Injection and the Rubber Wrapping

Start date: November 1, 2021
Phase: N/A
Study type: Interventional

This study is a prospective, multicentre, and randomized-controlled clinical study.The researchers wanted to explore the optimal treatment regimen for soft hemorrhoid within I-Ⅲ degrees by evaluating and comparing the effectiveness, safety and cost effect ratio of sclerosing injection and rubber lap ligation in patients with different internal hemorrhoid scores

NCT ID: NCT04881344 Not yet recruiting - Hemorrhoids Clinical Trials

Mucopexy Versus Laser Hemorrhoidoplasty for the Treatment of Hemorrhoidal Disease

MuLa
Start date: June 2021
Phase: N/A
Study type: Interventional

Hemorrhoidal disease is a frequent anorectal disorder and the main reason for a visit to a coloproctologist. Hemorrhoids are present in healthy individuals. However, they can become pathologic, manifesting with pain, prolapse, itching, bleeding or soiling. Initially, they can be managed conservatively. When this failed to cure the symptoms, surgical therapy is indicated. For grade II (hemorrhoids prolapsing during straining but reducing spontaneously) or grade III (hemorrhoids prolapsing during straining but requiring manual reduction), laser hemorrhoidoplasty or mucopexy are safe and efficient procedures to treat hemorrhoids. However, the optimal treatment is still under debate. Recently, a randomized controlled trial reported lower recurrence and faster return to work associated with laser therapy. We aimed to compare both therapies, to assess the benefits of laser therapy for the treatment of hemorrhoidal disease symptoms, using a validated score.

NCT ID: NCT04362384 Not yet recruiting - Pain Clinical Trials

Topical Vitamin E Ovules for the Treatment of Hemorrhoids

Start date: May 1, 2020
Phase: Phase 3
Study type: Interventional

Patients with hemorrohoids grade II and III were included. Patients were randomized into 2 groups: - Experimental group: Patients will receive a treatment with vitamin E ovules, which must be placed inside the annus - Control group: Patients will receive a treatment with corticoid ointment, with endoanal application Bleeding, pain and stinging will be evaluated 14 days after beginning the treatment.

NCT ID: NCT04101773 Not yet recruiting - Hemorrhoids Clinical Trials

Napoleon Trial: Optimal Treatment for Recurrent Haemorrhoidal Disease

Start date: March 1, 2020
Phase: N/A
Study type: Interventional

Rationale: There is level I evidence in literature that the first management step of HD is basic treatment, including laxatives and high fibre dieti, ii. The next treatment modality after basic treatment in case of persistent symptoms is rubber band ligation (RBL), which can be repeated if necessary. There is currently no consensus and a lack of evidence regarding the best treatment option for these patients having recurrent HD: continuing RBL or a surgical intervention. Furthermore, there is no estimate of costs and cost-effectiveness in this patient group. Objective: The primary objective of this RCT is to compare the effectiveness of RBL, sutured mucopexy and haemorrhoidectomy regarding recurrence and patient-reported symptoms for recurrent grade 2 and 3 HD after at least 2 previous RBL treatments. Secondary objectives are to compare RBL, sutured mucopexy and haemorrhoidectomy for recurrent grade 2 and 3 HD after previous RBL treatments in terms of early and late complications, impact of symptoms on daily activities, patient satisfaction with treatment, health-related quality of life, costs and cost-effectiveness, and budget impact. Study design: Dutch prospective multicentre randomized controlled trial. Study population: Patients ≥18 who have recurrent grade 2 or 3 haemorrhoidal disease and who had at least 2 rubber band ligation treatments. In total, 558 patients will be included. Intervention: Rubber band ligation versus sutured mucopexy versus haemorrhoidectomy. All three interventions are part of Dutch usual care, and serve as each other's control. Main study parameters/endpoints: Primary outcomes are (1) recurrence and (2) patient-reported symptoms assessed after 12 months. Secondary outcome variables are early and late complications, impact of symptoms on daily activities, patient satisfaction with treatment, health-related quality of life, costs, cost-effectiveness and budget-impact.

NCT ID: NCT03805087 Not yet recruiting - Hemorrhoids Clinical Trials

Transarterial Coil Embolization of the Superior Rectal Arteries for Treatment of Stage II Hemorrhoids

Start date: January 2019
Phase: N/A
Study type: Interventional

This study will evaluate short , mid and long term efficacy of transarterial coil embolization of the superior rectal arteries (Emborrhoid techinque) for treatment the hemorrhoidal disease.

NCT ID: NCT03780998 Not yet recruiting - Hemorrhoids Clinical Trials

Effects of Sodium Pentaborat Based Gel on Perianal Benign Diseases

Start date: January 1, 2019
Phase:
Study type: Observational

New produced and patented sodium pantaborat based gel will be use for treatment of benign perianal diseases (hemooroidal disease, anal fissura anda perianal fistula)

NCT ID: NCT02579330 Not yet recruiting - Hemorrhoids Clinical Trials

Trial on Use of Coloshield in Transanal and Anal Surgery

Start date: December 2015
Phase: N/A
Study type: Interventional

In various transanal and anal procedures it is desirable to clean the operating field from stool contamination. Thus mechanical bowel preparation is not well tolerated by patients. Enema does not provide sufficient effect. By the use of Coloshield a rectal washout might be performed and enable a clean operating field. In this randomized controlled trial the macroscopic contamination of the rectum with and without Coloshield is compared using the Boston Bowel Preparation Score (0-3).

NCT ID: NCT02295592 Not yet recruiting - Hemorrhoids Clinical Trials

TSTstarr + for Treatment of Severe Prolapsed Hemorrhoids --- a Multi-center Randomized Controlled Clinical Trail

Start date: November 2014
Phase: N/A
Study type: Interventional

TSTstarr+ in the treatment of severe hemorrhoids prolapse--A multi center randomized controlled clinical trial.The aim of this stuy is to compare the first year hemorrhoids recurrence rate of TSTstarr+ and PPH in the treatment of severe hemorrhoids.

NCT ID: NCT02039570 Not yet recruiting - Haemorrhoids Clinical Trials

The Relationship Between Haemorrhoids and Pelvic Vein Reflux

Start date: March 2014
Phase: N/A
Study type: Observational

This case series aims to find out in a group of female patients suffering from haemorrhoids, how many of them have pelvic vein reflux that feeds into their haemorrhoids. This will be done by examining their ovarian and internal iliac veins for reflux, using a transvaginal scan.

NCT ID: NCT01321619 Not yet recruiting - Hemorrhoids Clinical Trials

Efficacy and Tolerability of the Use of Varicell Compared With Daflon

Start date: July 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and tolerability of Varicell compared to Daflon, in reducing the symptoms caused by chronic venous insufficiency and hemorrhoidal syndrome.