Evaluation of Chamomile on complications of internal sphincterotomy for chronic anal fissure

Evaluation of traditional preparation of Chamomile on complications of internal sphincterotomy for chronic anal fissure: A double blind clinical trial

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20220521054941N1

Enrollment

Registered

2024-08-04

Start date

2024-08-22

Completion date

Unknown

Last updated

2024-08-26

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

Conditions

Internal Sphinctrotomy for chronic anal fissure.

Interventions

Intervention 1: Intervention group: includes patients who have undergone sphincterotomy and use chamomile traditional medicine product in the form of a douche (placing the perineal area in a basin of

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Male or female patients over 18 years of age who have undergone sphincterotomy due to anal fissures.

Exclusion criteria

Exclusion criteria: Dissatisfaction Inability to fully cooperate during study Allergy to chamomile Bleeding Other diseases that involve the perineum

Design outcomes

Primary

Measure	Time frame
Inflamation. Timepoint: After the operation and at intervals of two, four and eight weeks later. Method of measurement: The checklist was completed by the researcher after the examination and evaluation of the patients by the general surgeon.	—

Secondary

Measure	Time frame
Relapse. Timepoint: After the operation and at intervals of two, four and eight weeks later. Method of measurement: The checklist was completed by the researcher after the examination and evaluation of the patients by the general surgeon.;Pain. Timepoint: After the operation and at intervals of two, four and eight weeks later. Method of measurement: The checklist was completed by the researcher after the examination and evaluation of the patients by the general surgeon.;Bleeding. Timepoint: After the operation and at intervals of two, four and eight weeks later. Method of measurement: The checklist was completed by the researcher after the examination and evaluation of the patients by the general surgeon.;Infection. Timepoint: After the operation and at intervals of two, four and eight weeks later. Method of measurement: The checklist was completed by the researcher after the examination and evaluation of the patients by the general surgeon.;Wound healing. Timepoint: After the operation and at intervals of two, four and eight weeks later. Method of measurement: The checklist was completed by the researcher after the examination and evaluation of the patients by the general surgeon.;Burning and skin sensitivity. Timepoint: After the operation and at intervals of two, four and eight weeks later. Method of measurement: The checklist was completed by the researcher after the examination and evaluation of the patients by the general surgeon.	—

Measure

Time frame

Relapse. Timepoint: After the operation and at intervals of two, four and eight weeks later. Method of measurement: The checklist was completed by the researcher after the examination and evaluation of the patients by the general surgeon.;Pain. Timepoint: After the operation and at intervals of two, four and eight weeks later. Method of measurement: The checklist was completed by the researcher after the examination and evaluation of the patients by the general surgeon.;Bleeding. Timepoint: After the operation and at intervals of two, four and eight weeks later. Method of measurement: The checklist was completed by the researcher after the examination and evaluation of the patients by the general surgeon.;Infection. Timepoint: After the operation and at intervals of two, four and eight weeks later. Method of measurement: The checklist was completed by the researcher after the examination and evaluation of the patients by the general surgeon.;Wound healing. Timepoint: After the operation and at intervals of two, four and eight weeks later. Method of measurement: The checklist was completed by the researcher after the examination and evaluation of the patients by the general surgeon.;Burning and skin sensitivity. Timepoint: After the operation and at intervals of two, four and eight weeks later. Method of measurement: The checklist was completed by the researcher after the examination and evaluation of the patients by the general surgeon.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehrangiz Ansari dezfuli

Kerman University of Medical Sciences

ansarimehr1400z@gmail.com+98 34 3243 0653

Outcome results

None listed

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