Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:17 PM
Ignite Modification Date:
2026-03-26 @ 3:17 PM
NCT ID:
NCT07369635
Eligibility Criteria:
\- Inclusion Criteria
Patients must meet all of the following criteria to be eligible for the study:
* Age 18 to 65 years
* Diagnosis of grade II internal hemorrhoids with bleeding, presenting with the following symptoms:
Hemorrhoids prolapse with gentle straining and retract spontaneously Presence of blood in stool Congested and/or bleeding hemorrhoids
* Having symptoms such as anal pain and anal itching
* Willingness to voluntarily participate in the study - Exclusion Criteria
Patients meeting any of the following criteria will be excluded from the study:
* History of malignancy, including colon cancer and other cancers
* Anal polyps and proctitis
* Anal fissures with bleeding
* Systemic diseases, such as hypertension, liver failure, kidney failure, heart failure, and coagulation disorders.
* Other severe acute or chronic illnesses
* Mixed hemorrhoids or conditions requiring immediate surgical intervention, such as hematoma, severe bleeding, or hemorrhoidal infarction
* Recent use of other hemorrhoid medications (within 7 days prior to study enrollment)
* Known allergy to any component of the study medications
* Pregnant or lactating women
* Patients will be withdrawn from the study if they: Do not adhere to the treatment regimen, including missing medication for more than 3 consecutive days. Or Use other prohibited medications during the study period. Or require routine medical care at the hospital due to non-compliance or other medical reasons.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT07369635
Study Brief:
Protocol Section:
NCT07369635