Safety and Efficacy Study of HET Bipolar System for Treatment of Stage I and Stage II Hemorrhoids
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|ClinicalTrials.gov Identifier: NCT01841970|
Recruitment Status : Completed
First Posted : April 29, 2013
Results First Posted : January 16, 2017
Last Update Posted : January 16, 2017
Hemorrhoids are vascular cushions in the anal canal. People are normally born with hemorrhoids, and the presence of hemorrhoids does not imply disease. However, hemorrhoids typically cause symptoms when they enlarge over time. There are two types of hemorrhoids- External Hemorrhoids and Internal Hemorrhoids.
Current minimally invasive technologies for the treatment of internal hemorrhoids are associated with several drawbacks that include high rate of recurrence and a need for repetitive procedures, frequent post-procedural pain or significant discomfort, intra-operative pain and technically demanding. The purpose of this study is to determine whether the HET Bipolar System is safe and effective in the treatment of Stage I and Stage II hemorrhoids (internal hemorrhoids). The HET Bipolar System is a new alternative device for the minimally invasive treatment of Stage I and Stage II hemorrhoids that incorporate design features with the intent of resolving each of the major limitations of currently available technology.
|Condition or disease||Intervention/treatment||Phase|
|Hemorrhoids, Internal||Device: HET Bipolar System||Not Applicable|
In this study, the investigators will use the HET Bipolar System for the treatment of Stage I and Stage II hemorrhoids, where significant tissue prolapse is not present. The hemorrhoids are treated by bipolar ligation of the superior hemorrhoidal blood supply.
Each prospective subject will be screened for inclusion and exclusion criteria at least one week prior to treatment. All patients undergoing treatment will review and sign the study Informed Consent prior to their procedure.
One to three internal hemorrhoids will be treated in one therapeutic session. The number will be based on the investigator's judgment of which quadrants are symptomatic. Evaluations will be recorded for all treated subjects immediately following treatment. Subjects will be followed at 1, 3, and 6 months post procedure unless complications are reported between scheduled follow-up dates. At each post treatment follow-up, a report will be made of pain/discomfort, bleeding, medication use, itching, presence of adverse events or complications and need for supplemental treatment. Face-to-face follow-up evaluations will include anoscopic evaluation and assessment of hemorrhoid and other relevant symptoms.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||20 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Multi-Center, Prospective Study of the Safety and Efficacy of the HET Bipolar System for Treatment of Stage I and Stage II Hemorrhoids|
|Study Start Date :||April 2013|
|Actual Primary Completion Date :||November 2014|
|Actual Study Completion Date :||January 2015|
Active arm. A single procedure with HET was used to treat Grade I and Grade II hemorrhoids
Device: HET Bipolar System
The HET Bipolar System is used to treat hemorrhoids by bipolar ligation of the superior hemorrhoidal blood supply.
- Number of Participants With Resolution of Symptoms [ Time Frame: Post treatment at Month1, Month 3, Month 6 ]The primary endpoint analysis was the resolution of symptoms, including resolution of bleeding and prolapse, if present prior to treatment
- Incidence of Recurrence of Pre-procedure Symptoms [ Time Frame: Post treatment at Month 1, Month 3, and Month 6 ]Recurrence of pre-procedure symptoms after initial improvement
- Recurrence of Symptoms That Had Resolved With Treatment [ Time Frame: Post treatment at Month 1, Month 3, Month 6 ]Number of patients with recurrence of symptoms defined as external thrombosed hemorrhoids, infection, mucous discharge, new fissure, stenosis and delayed healing.
- Pain Recorded Yes or No on Visual Analog Scale (VAS) [ Time Frame: Post treatment at Month 1, Month 3, Month 6 ]Patient reported pain on 10 point scale where 0 =No Pain and > 0 = Pain with 10 being the worst.
- Mean Pain Score Based on the Visual Analog Pain Scale [ Time Frame: Post treatment at Month 1, Month 3, Month 6 ]Mean pain score based on the Visual Analog pain scale. Patient reported pain on 10 point scale where 0 =No Pain and > 0 = Pain with 10 being the worst.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01841970
|United States, Ohio|
|University Hospitals Case Medical Center|
|Cleveland, Ohio, United States, 44106|