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The study on role of gooseberry (Amla) reducing the size of uterine fibroids

Evaluating the efficacy of Amla(Emblica officinalis gaertn) in the management of uterine fibroids - Nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110226
Enrollment
40
Registered
2026-05-08
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: N711- Chronic inflammatory disease of uterus

Interventions

Intervention1: Powder of Amla: Patient will be given oral medicine powder of Amla ( Emblica officinalis gaertn) in capsule form 6 gm with normal water in three divided doses from D-6 to D-25 of cycle

Sponsors

Government Nizamia tibbi college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Female patients age between 20 to 45 years Unmarried married and non pregnant Diagnosed cases of uterine fibroids and not resolved cases after treatment Uterine fibroids one to multiple (1 to 5) less than 5 centimeter USG report Symptomatic fibroids (intramural) Controlled diabetes mellitus (RBS less than 200 HbA1c 6.4 percent FBS 70 to 99 milligram per decilitre and PLBS less than 140 milligram per decilitre Controlled hypertension less than 130 over 80 mmHg Patients who is ready to participate in the study and who are willing to sign consent form

Exclusion criteria

Exclusion criteria: Women who attained menopause Pregnant and lactating women Uterine fibroid greater than 5 centimeter Severe anemia (Hb less than 8.0 gram per decilitre) Women with high risk cases like severe cardiac diseases hepato renal diseases and respiratory diseases Combined with malignant tumors including reproductive and other systems Patients with co morbidities (un controlled hypertension and uncontrolled diabetes mellitus)

Design outcomes

Primary

MeasureTime frame
To assess improvements in fibroid associated symptoms (VAS PBAC UFS QoL( specifically 6 12 point scale) ( pre and post treatment)Timepoint: 0th day and 90th day

Secondary

MeasureTime frame
To reduce the uterine fibroid size (USG report) (pre and post treatment) To evaluate safety and tolerability of the treatment Timepoint: Baseline 0 Day 90

Countries

India

Contacts

Public ContactDr Nishath parveen

Government Nizamia tibbi college and general hospital

syedaabidunnisa@gmail.com9492027082

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026