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Clinical Trial of Karpura Ghruta in Post Haemorrhoidectomy Wound Management

Randomized Controlled Clinical Trail of Karpura Ghruta in Post Haemorrhoidectomy Wound Management

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/02/017627
Enrollment
100
Registered
2019-02-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: L768- Other intraoperative and postprocedural complications of skin and subcutaneous tissue

Interventions

Intervention1: Karpura Ghruta: Local application of karpura ghruta on Post Haemorrhoidectomy Wound and Surgical(shashtrakshata)wound once daily for 15 days. Control Intervention1: Metro-P ointment: Lo

Sponsors

Amit Ramesh Satvi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient will be selected Irrespective of sex,religion, marital status,education and economic status. 2.Patient operated for third and fourth degree haemorrhoids without any complication 3.Patient who have undergone elective Procedure. 4.Patient who are willing to Participate

Exclusion criteria

Exclusion criteria: 1.Patient of Haemorrhoids with major illness. 2.Patient of Haemorrhoids with associated diseases like, Prolapse of rectum, Ca-rectum 3.Immunocompromised patient. 4.Non-cooperative Patient.

Design outcomes

Primary

MeasureTime frame
1.To study the effect of Karpura Ghruta on Post Haemorrhoidectomy Wound 2.To compare the analgesic property and rate of wound healing of Karpur Ghruta and Metro-P ointment in Post Haemorrhoidectomy wound.Timepoint: 15 days.

Secondary

MeasureTime frame
1.To assess the effect of Karpura Ghruta on various clinical feature of Wound like Pain, tenderness, discharge and duration of the wound Healing.Timepoint: 15 days

Countries

India

Contacts

Public ContactDr Nita Kedar

Government Ayurved College and Hospital

drnita6@gmail.com9422117613

Outcome results

None listed

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