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Evaluating the Impact of Tikataka Ghrita Matra Basti in Treating Adenomyosis: A Clinical Study

A CLINICAL STUDY TO EVALUATE THE EFFECT OF TIKTAKA GHRITA MATRA BASTI IN THE MANAGEMENT OF ASRIGDARA (ADENOMYOSIS) - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/075370
Enrollment
30
Registered
2024-10-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: N738- Other specified female pelvic inflammatory diseases

Interventions

None listed

Sponsors

Rohini Ghuguskar
Lead Sponsor
Dr Swathi C
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Age group between 35 to 50 years Diagnosed cases of Adenomyosis with the Heavy Menstrual Bleeding and Dysmenorrhoea.

Exclusion criteria

Exclusion criteria: Use of IUCD Patient with ongoing treatment of systemic disease like diabetes, hypertension, cardiac diseases. Polyps, Leiomyoma, Malignancy and hyperplasia, Coagulopathy, Ovulatory dysfunction, Endometrial, Iatrogenic. Endocrinal Diseases (Hypo/ Hyper Thyroidism) Non - menstrual causes for bleeding (Foreign body, Abortion) Hb percentage less than 7 PCOS

Design outcomes

Primary

MeasureTime frame
Reduction in Menstrual Bleeding: Measured as the change in the volume, duration, and frequency of menstrual bleeding. This can be assessed using a combination of patient-reported outcome measures (such as menstrual diaries or questionnaires) and clinical assessments (such as blood loss quantification and imaging studies) before and after the intervention.Timepoint: 6 days in a month for three consecutive cycles

Secondary

MeasureTime frame
Menstrual Pain Severity: Assessment of changes in the severity of menstrual pain using a standardized pain scale (e.g., Visual Analog Scale or Numeric Rating Scale).Menstrual Bleeding: Evaluation of changes in menstrual bleeding patterns, including duration and volume of menstrual flow.Quality of Life: Measurement of improvements in overall quality of life related to symptoms of adenomyosis, using a validated quality of life questionnaire.Hormonal Profile: Analysis of hormonal changes related to adenomyosis, such as levels of estrogen and progesterone.Adverse Events: Monitoring and reporting of any adverse events or side effects associated with the treatment.Patient Satisfaction: Assessment of patient satisfaction with the treatment regimen and perceived improvements in symptoms.Uterine Size: Measurement of changes in uterine size through imaging techniques such as ultrasound or MRI.Timepoint: 6 days in a month for three consecutive cycles

Countries

India

Contacts

Public ContactGhuguskar Rohini Nilkanth

Sri Jayendra Saraswathi Ayurveda College and Hospital, Chennai

drswathi@sjsach.org.in8105774944

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 27, 2026