Hemorrhoid Artery LigatioN Without Doppler Trial (HAND)
Primary Purpose
Hemorrhoids
Status
Unknown status
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
doppler-guided hemorrhoidal artery ligation
Finger-guided hemorrhoidal artery ligation
Sponsored by
About this trial
This is an interventional treatment trial for Hemorrhoids focused on measuring hemorrhoids, hemorrhoidal piles, prolapse, doppler guided ligation, finger-guided artery ligation
Eligibility Criteria
Inclusion Criteria:
- Symptomatic grade II and III hemorrhoids according to Golligher.
- No other source of anal bleeding than hemorrhoids due to total colonoscopy
- Written voluntary informed consent
Exclusion Criteria:
- Any previous hemorrhoid surgery (including mini invasive procedures)
- Anal fistula
- Chronic anal fissure with severe spasm of anal sphincters
- Any stage colorectal cancer
- Oral anticoagulants for congenital disorders of the coagulation system
- Pregnancy
Sites / Locations
- Clinic of Colorectal and Minimally invasive surgeryRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
doppler-guided
finger-guided group
Arm Description
ligation of hemorrhoidal arteries with doppler guidance
ligation of hemorrhoidal arteries without doppler guidance but with finger detection
Outcomes
Primary Outcome Measures
recurrence
The rate of recurrence of any of initial symptoms or appearance of any new symptom of hemorrhoidal disease: anal bleeding during defecation, prolapse of hemorrhoidal piles or both.
Secondary Outcome Measures
Pain score
pain score after surgery will be measured by patient-reported pain level using visual scale ranging from 1 to 10 where 1 is "no pain" and 10 - is the the worst pain imaginable.
Patients satisfaction level
Patients will be asked to rate their own satisfaction of the procedure on a scale from 1 to 10 (with 10 being the best) and were asked whether the procedure helped their symptoms.
Full Information
NCT ID
NCT04119401
First Posted
October 6, 2019
Last Updated
March 24, 2020
Sponsor
Russian Society of Colorectal Surgeons
1. Study Identification
Unique Protocol Identification Number
NCT04119401
Brief Title
Hemorrhoid Artery LigatioN Without Doppler Trial
Acronym
HAND
Official Title
Hemorrhoidal Artery Ligation With Doppler Guidance vs Digital Guidance for Grade II-III Hemorrhoidal Disease Treatment: Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
March 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 8, 2019 (Actual)
Primary Completion Date
October 10, 2020 (Anticipated)
Study Completion Date
January 11, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Russian Society of Colorectal Surgeons
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Hemorrhoidal artery ligation with Doppler guidance (HAL) and suture fixation of hemorrhoidal nodes (RAR) is a popular minimally invasive technique for hemorrhoidal disease (HD) treatment which uses an ultrasound probe to detect hemorrhoidal arteries for further ligation. We hypothesized that ultrasound guidance has no advantages over manual hemorrhoidal arteries detection for HD treatment.
The aim is to compare the results of HAL-RAR procedure in patients with stage II-III HD with Doppler and manual HA detection.
In this ongoing randomized, controlled, single center clinical study 200 patients randomly divided into group A (HAL-RAR with Doppler US navigation) and group B (HAL with manual HA detection and mucopexy) are planned to be included. The primary endpoint was recurrence of any symptoms of HD; secondary endpoints were pain syndrome severity (VAS), treatment satisfaction (1 to 5 points) and need for the drug therapy in 30 days and 8 weeks after surgery.
Ultrasound guidance technology of HAL with mucopexy could have the same efficacy the manual HA detection regarding the HD treatment effectiveness and patient satisfaction.
Detailed Description
Hemorrhoidal disease (HD), in its different manifestations, is not only the most frequented grounds of referring for medical attention, but also one of the reasons for the modest deterioration in the quality of life that can possibly result in temporary or permanent reduction of work capacities. Today, the doppler-guided dearterialization of hemorrhoidal arteries and the following suture-fixation mucopexy in the anal canal (synonyms: mucopexy, hemorrhoids lifting, HAL-RAR) is one of the most popular and actively studied methods of the stage II - III hemorrhoidal disease surgical treatment. A number of publications raise an issue whether it is really necessary to use a doppler while the localization of the hemorrhoidal arteries is typical in the vast majority of the observations and can be easily determined on palpation.
The aim of the study is to compare the direct and long-term results of the II - III grade HD surgical treatment with the use of two techniques of the suture ligation of the hemorrhoidal arteries with mucopexy. One of these methods is classic and widely known HAL-RAR, the other one has a principal differ in no-using the doppler to find the arteries, the surgeon defines them on palpation.
The hypothesis of the study is that the digital detection of hemorrhoidal arteries pulsation followed by suture ligation and mucopexy may be no less effective in the treatment of grade II - III hemorrhoids than the use of a doppler guide.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemorrhoids
Keywords
hemorrhoids, hemorrhoidal piles, prolapse, doppler guided ligation, finger-guided artery ligation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
doppler-guided
Arm Type
Active Comparator
Arm Description
ligation of hemorrhoidal arteries with doppler guidance
Arm Title
finger-guided group
Arm Type
Experimental
Arm Description
ligation of hemorrhoidal arteries without doppler guidance but with finger detection
Intervention Type
Procedure
Intervention Name(s)
doppler-guided hemorrhoidal artery ligation
Intervention Description
Ligation: a lubricating gel is applied to the tip of the Transanal Hemorrhoidal Dearterialization device and, with the patient in the lithotomy position, the proctoscope is introduced into the anal canal. The terminal branches of the superior rectal artery are detected by the doppler signal 2-3 cm above the dentate line. The tip of the instrument is gently tilted and the arteries are ligated with a Z-shaped stitch using 2:0 braided polyglycolic acid suture inserted using a special needle-holder through an aperture in the operating proctoscope.
Mucopexy: after the haemorrhoid artery ligation, the suture is continued with three to five sutures applied 5 mm apart, making sure that the last is at least 5 mm above the dentate line. The suture is then tied to create a hemorrhoidopexy. The procedure is repeated after all detected artery ligations.
Intervention Type
Procedure
Intervention Name(s)
Finger-guided hemorrhoidal artery ligation
Intervention Description
Ligation: the exact placement of all terminal branches of the superior rectal artery are found by intraoperative palpation at anal clock 2-3cm above the anorectal junction. Then arteries are ligated with Z-shaped suture using 2:0 braided polyglycolic suture.
Mucopexy is then performed in the same technique as in comparative group
Primary Outcome Measure Information:
Title
recurrence
Description
The rate of recurrence of any of initial symptoms or appearance of any new symptom of hemorrhoidal disease: anal bleeding during defecation, prolapse of hemorrhoidal piles or both.
Time Frame
2 weeks - 1 year
Secondary Outcome Measure Information:
Title
Pain score
Description
pain score after surgery will be measured by patient-reported pain level using visual scale ranging from 1 to 10 where 1 is "no pain" and 10 - is the the worst pain imaginable.
Time Frame
2 weeks
Title
Patients satisfaction level
Description
Patients will be asked to rate their own satisfaction of the procedure on a scale from 1 to 10 (with 10 being the best) and were asked whether the procedure helped their symptoms.
Time Frame
6 month and 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Symptomatic grade II and III hemorrhoids according to Golligher.
No other source of anal bleeding than hemorrhoids due to total colonoscopy
Written voluntary informed consent
Exclusion Criteria:
Any previous hemorrhoid surgery (including mini invasive procedures)
Anal fistula
Chronic anal fissure with severe spasm of anal sphincters
Any stage colorectal cancer
Oral anticoagulants for congenital disorders of the coagulation system
Pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Daniil Markaryan, MD
Phone
+79035329245
Email
markaryan@kkmx.ru
First Name & Middle Initial & Last Name or Official Title & Degree
Inna Tulina, MD
Phone
+79264086672
Email
tulina@kkmx.ru
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Petr Tsarkov, Prof
Organizational Affiliation
Russian Society of Colorectal Surgeons
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinic of Colorectal and Minimally invasive surgery
City
Moscow
ZIP/Postal Code
119435
Country
Russian Federation
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Inna Tulina, MD
Phone
+79264086672
Email
tulina@kkmx.ru
First Name & Middle Initial & Last Name & Degree
Petr Tsarkov, PhD
First Name & Middle Initial & Last Name & Degree
Markaryan Daniil, MD
First Name & Middle Initial & Last Name & Degree
Mikhail Bredikhin, MD
First Name & Middle Initial & Last Name & Degree
Tatiana Garmanova, MD
First Name & Middle Initial & Last Name & Degree
Aftandil Alikperzade, MD
12. IPD Sharing Statement
Citations:
PubMed Identifier
14706597
Citation
Aigner F, Bodner G, Conrad F, Mbaka G, Kreczy A, Fritsch H. The superior rectal artery and its branching pattern with regard to its clinical influence on ligation techniques for internal hemorrhoids. Am J Surg. 2004 Jan;187(1):102-8. doi: 10.1016/j.amjsurg.2002.11.003.
Results Reference
result
PubMed Identifier
27236344
Citation
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.
Results Reference
result
PubMed Identifier
26876958
Citation
Hoyuela C, Carvajal F, Juvany M, Troyano D, Trias M, Martrat A, Ardid J, Obiols J. HAL-RAR (Doppler guided haemorrhoid artery ligation with recto-anal repair) is a safe and effective procedure for haemorrhoids. Results of a prospective study after two-years follow-up. Int J Surg. 2016 Apr;28:39-44. doi: 10.1016/j.ijsu.2016.02.030. Epub 2016 Feb 10.
Results Reference
result
PubMed Identifier
7717320
Citation
Morinaga K, Hasuda K, Ikeda T. A novel therapy for internal hemorrhoids: ligation of the hemorrhoidal artery with a newly devised instrument (Moricorn) in conjunction with a Doppler flowmeter. Am J Gastroenterol. 1995 Apr;90(4):610-3.
Results Reference
result
PubMed Identifier
29170839
Citation
Ratto C, Campenni P, Papeo F, Donisi L, Litta F, Parello A. Transanal hemorrhoidal dearterialization (THD) for hemorrhoidal disease: a single-center study on 1000 consecutive cases and a review of the literature. Tech Coloproctol. 2017 Dec;21(12):953-962. doi: 10.1007/s10151-017-1726-5. Epub 2017 Nov 24. Erratum In: Tech Coloproctol. 2018 Feb 28;:
Results Reference
result
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Hemorrhoid Artery LigatioN Without Doppler Trial
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