Skip to content

Comparison of the three types of medical treatment; Topical application of Nitroglycerin plus Diltiazem Gel , Bethanechol Gel and Diltiazem Gel in healing chronic anal fissure

Effect of topical application of Nitroglycerin plus Diltiazem compared with the two methods of topical use of Bethanechol and Diltiazem in the treatment of patients with chronic anal fissure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016110130623N1
Enrollment
90
Registered
2017-09-13
Start date
2016-10-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic anal fissure. chronic anal fissure

Interventions

Intervention 1: Interventional group 1: Combination therapy (1% Nitroglycerine ointment plus topical 5% Diltiazem gel as separate product), TDS for eight weeks. Intervention 2: Intervention group 2: b
Treatment - Drugs
Interventional group 1: Combination therapy (1% Nitroglycerine ointment plus topical 5% Diltiazem gel as separate product), TDS for eight weeks
Intervention group 2: bethanechol , 0.1% gel, topical, TDS for eight weeks
Control group: diltiazem, 5% gel, topical, TDS for eight weeks

Sponsors

Vice Chancellor for research of Kurdistan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: for this study does not consider specific criteria except having acute fissures. Exclusion Criteria: pregnancy; Inflammatory bowel disease; The incidence of side effects; Leave treatment; Colon cancer

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Healing of fissure. Timepoint: Before intervention , 4 and 8 weeks after intervention. Method of measurement: Examination.

Secondary

MeasureTime frame
Bleeding. Timepoint: Before intervention, 4 and 8 weeks after intervention. Method of measurement: Examination and question from the patient.;Pain. Timepoint: Before intervention , 4 and 8 weeks after intervention. Method of measurement: Examination and question from the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBaran Parhizkar

Liver & Digestive Research center,Kurdistan university of medical sciences

b.parhizkar@muk.ac.ir+98 87 3366 4645

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026