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Liver DiseasesNCT04535440

To Describe the Clinical, Endoscopic and Endoscopic Ultrasound Features of Non-bleeding and Bleeding Rectal Varices, Among Patients With Portal Hypertension

An observational study of Liver Diseases, run by Institute of Liver and Biliary Sciences, India at 1 site in India.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Rectal varices (RVs) are an important cause of lower gastrointestinal bleed (LGIB) in portal hypertension (PHT) and have been reported to occur in 44% to 89% of cases of cirrhosis. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Liver Diseases
How many people
100 participants
Where
1 siteIndia
Study dates
7 Jan 2021to 31 Jul 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: All patients with PHT (cirrhotic or non-cirrhotic), with active or prior anorectal bleeding (defined later) in the preceding 6-months will be evaluated for inclusion. We will also include patients with incidental detection of RV during endoscopy done for other indications. We will include both indoor and outdoor patients, attending the Department of Hepatology, ILBS, New Delhi. An informed consent will be obtained from the participants in the study.

Who may be able to join

  • Age >18-years.
  • Patients with PHT and active or prior anorectal bleeding in preceding 6-months.
  • Patients with RV (bleeding or non-bleeding) detected on LGI endoscopy.
  • Ability to understand study procedures, and to comply with them for the entire length of the study.

Who cannot join

  • Peri-anal infection, peri-anal warts, anal condyloma, or fistulizing disease.
  • Proctitis- infective, inflammatory bowel disease (IBD), radiation, or unspecified.
  • Pregnant or lactating females.
  • Presence of hemodynamic instability.
  • Presence of encephalopathy
  • Non-consenting adult patient or guardian.
  • Prior history of banding or surgery for hemorrhoids, or endotherapy for RV.
  • Prior shunt occlusion procedures like BRTO or PARTO, or shunt creation procedures like TIPS.

Trial locations and contacts

1 site in 1 country.

Dr Hitesh Singh, MD contact

01146300000

hiteshrims04@gmail.com

India1 site, 1 recruiting
  • Institute of Liver & Biliary Sciences

    New Delhi, National Capital Territory of Delhi, 110070

    Dr Hitesh Singh, MD, 01146300000, hiteshrims04@gmail.com

    Recruiting

Other trials in India

About this study

Official title: To Describe the Clinical, Endoscopic and Endoscopic Ultrasound Features of Non-bleeding and Bleeding Rectal Varices, Among Patients With Portal Hypertension.

Rectal varices (RVs) are an important cause of lower gastrointestinal bleed (LGIB) in portal hypertension (PHT) and have been reported to occur in 44% to 89% of cases of cirrhosis. RVs are dilated sub-mucosal porto-systemic communications which extend from mid rectum to the ano-rectal junction and are considered distinct from internal hemorrhoids, which are submucosal arterio-venous communications of the anorectal vascular plexus. The suspicion of RVs as the cause of bleeding can be made with a high index of suspicion when lower GI bleed is seen in absence of hemorrhoids, and colonoscopy shows blood in rectum. Bleeding usually happens from endoscopically evident rectal varices (EERV) but sometimes bleed can occur from varices, which are endoscopically in evident (EIERV). Endoscopic ultrasound (EUS) has been shown to be more sensitive in diagnosis of EIERV. Endoscopic and EUS correlation of RVs has shown that RVs, classified as tortuous, nodular, and tumorous on endoscopic examination, have corresponding appearances on rectal EUS as single, multiple, and innumerable submucosal veins, respectively. The hemodynamic evaluation (HDE) of RVs by EUS is routinely done at some centers to assess parameters like the site, size, velocity, or direction of flow.

Read the detailed description

AIM:

To describe the clinical, radiological, endoscopic and endoscopic-ultrasound features of non-bleeding and bleeding rectal varices, among patients with portal hypertension.

OBJECTIVES:

Primary objectives:

Anatomical and liver -related risk-factors for presence of rectal varices (RV) among patients with portal hypertension Secondary objectives

  1. Etiological spectrum of bleeding per-rectum, among patients with PHT.
  2. Frequency of coexistence of hemorrhoids with RV.
  3. Distribution and size of variceal channels in the rectum on endoscopy and endoscopic ultrasound (EUS).
  4. Location and numbers of inflow and outflow perforator channels for RV on endoscopic ultrasound (EUS).

Patients and methodology

Study Population:

All patients with PHT (cirrhotic or non-cirrhotic), with active or prior anorectal bleeding (defined later) in the preceding 6-months will be evaluated for inclusion. We will also include patients with incidental detection of RV during endoscopy done for other indications. We will include both indoor and outdoor patients, attending the Department of Hepatology, ILBS, New Delhi. An informed consent will be obtained from the participants in the study.

Study Design Cross- sectional, observational and descriptive study

Study period September 2020 to February 2020. Baseline data

The following clinical, biochemical and radiological features will be recorded (detailed in the proforma):

  1. Liver disease etiology and severity, including Fibroscan and HVPG, where done.
  2. Upper endoscopy findings.
  3. Details of prior bleeding episodes if any (upper and lower).
  4. Details of current bleeding episodes.
  5. Radiological features (cirrhosis, splanchnic venous thrombosis, flow direction in portal vein (PV) and its tributaries, inferior mesenteric vein (IMV) diameter, enlarged para-rectal collateral circulation, large porto-systemic shunts).

Endoscopy protocol:

All patients will undergo a sigmoidoscopy or colonoscopy procedure, as per the clinical indication. Patients found to have RV will undergo EUS examination in addition. EUS evaluation of patients with hemorrhoids alone will be done at the discretion of the examiner after informed consent from the patient.

Bowel preparation: Patient will be advised liquid-soft diet for 24 hours before the examination day. Split dose PEG preparation (2-4 L volume) will be administered- 2L in evening before and 2L on day of procedure till 4hours before the study scheduled time.

Patient position: Left lateral position. Endoscopes: Colonoscope or gastroscope. EUS probes: Radial and linear EUS scopes, paired with Olympus compact EUS processor EU-M2.

Operators: Procto-sigmoidoscopy: HS supervised by VB/ VB EUS: VB/ HS supervised by VB

Study Definitions:

Lower GI bleeding LGIB will be defined as bleeding from a source distal to the ileocecal valve (24).

Acute lower gastrointestinal bleeding Acute LGIB will be defined as bleeding of recent duration (<3 days) that may result in hemodynamic instability, anemia, and/or the need for blood transfusion (25).

Clinically significant lower gastrointestinal bleeding[VB1] Requirement for blood transfusion, a hemoglobin drop of > 3g/dL from baseline or need for hospital admission.

A bleeding episode is clinically significant when there is (BAVENO III[VB2] ):

  1. Transfusion requirement of ≥ 2 units of blood within 24 hours of time zero, 2. Systolic blood pressure < 100 mmHg or a postural change of >20 mmHg, 3. Pulse rate >100/min at time zero Anorectal bleeding
  2. Anorectal bleeding will be defined as red bleed per-rectum without or with stool expulsion. In the latter instance it can be mixed with stools, may smear stool, may dribble after defecation, or may smear wipes.
  3. Anorectal bleeding may be painless or may be associated with pain.
  4. Anorectal bleeding may or may not be associated with hemodynamic changes.

Monitoring and assessment

Primary:

  1. Anatomical and liver -related risk-factors for presence of rectal varices (RV) among patients with portal hypertension

Secondary

  1. Etiological spectrum of bleeding per-rectum, among patients with PHT.
  2. Frequency of coexistence of hemorrhoids with RV.
  3. Distribution and size of variceal channels in the rectum on endoscopy and endoscopic ultrasound (EUS).
  4. Location and numbers of inflow and outflow perforator channels for RV on endoscopic ultrasound (EUS).

Statistical analysis The dependent variable in the study will be presence of RV, presence of large RV (>5mm), and RV bleeding. Independent variables will be presence/ absence of esophageal varices, gastric varices, ectopic varices, prior UGIE bleeding, prior endotherapy for esophago-gastric varices, ascites, gastro-lieno-renal shunt, other large porto-systemic shunt, PV and/or SV and/or SMV thrombosis or flow reversal, composite liver function scores (CTP and MELD), number, location, and size of rectal perforator channels, size of para-rectal collaterals, pulsatile/ phasic flow in perforator(s) and/or RV, and presence of hemorrhoids. The continuous data will be represented by Mean ± SD or by Median (IQR) as appropriate. The categorical data will be represented as frequency (%). Student t-test or Mann Whitney test will be used for quantitative data and Chi square test will be used for qualitative data. Besides this an appropriate statistical analysis like uni-variate and multi-variate logistic regression will be used at the time of data analyss. The significance will be seen at 5 %.

Adverse Event:

  1. Pain abdomen
  2. Bloating sensation
  3. Abdominal distension

Stopping Rule:No stopping rule

Ethical Issues in the study and plans to address these issues:No ethical issue related to my study

Conditions
Liver Diseases
Being tested
No intervention
Medical subject headings
Liver Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • No interventionOther

    No intervention

Study groups in NCT04535440
Study groupRoleWhat they receive
Rectal varices with bleedNot described
Receives: Other: No intervention
Rectal varices without bleedNot described
Receives: Other: No intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Anatomical and liver -related risk-factors for presence of rectal varices (RV) among patients with portal hypertension

    Measured: Day 1

Secondary outcomes (4)
  1. Etiological spectrum of bleeding per-rectum, among patients with PHT.

    Measured: Day 1

  2. Frequency of coexistence of hemorrhoids with Rectal varices

    Measured: Day 1

  3. Distribution and size of variceal channels in the rectum on endoscopy and endoscopic ultrasound (EUS).

    Measured: Day 1

  4. Location and numbers of inflow and outflow perforator channels for RV on endoscopic ultrasound (EUS).

    Measured: Day 1

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Sep 2020
  2. Study start7 Jan 2021
  3. Primary completion31 Jul 2022 (estimated)
  4. Study completion31 Jul 2022 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04535440
Sponsor's protocol ID
ILBS-PHT-01
Status last verified
Oct 2021
First submitted
27 Aug 2020
Last updated
12 Oct 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Liver Diseases, run by Institute of Liver and Biliary Sciences, India at 1 site in India.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 12 Oct 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in India. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Dr Hitesh Singh, MD (01146300000, hiteshrims04@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Anatomical and liver -related risk-factors for presence of rectal varices (RV) among patients with portal hypertension (time frame: Day 1). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Oct 2021.

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