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Optimal dose of centchroman in management of cyclical mastalgia

A prospective clinical study to determine the therapeutic dose of Centchroman in the manangement of cyclical mastalgia - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072215
Enrollment
100
Registered
2024-08-09
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: M95-M95- Other disorders of the musculoskeletal system and connective tissue

Interventions

Intervention1: centhroman in mastalgia: Centchroman given at dose of 30mcg per oral thrice/week for 4 weeks followed by 2/week for next 4 weeks followed by 1/week for next 4 weeks. Control Interventio

Sponsors

Uttar Pradesh University of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All women with mastalgia with VAS score =3 lasting for more than 5-7 days per cycle were included after signing a consent form.

Exclusion criteria

Exclusion criteria: • Patients with polycystic ovarian diseases and uterine cervical hyperplasia. • First six months of Lactation and pregnancy • Patients who were not giving consent. • Past history of breast carcinoma or family history of breast carcinoma • Patient who were planning for pregnancy . • Women suspected or diagnosed of malignancy • Recent history of jaundice or hepatic impairment. • Severe allergic states. • History of thrombosis.

Design outcomes

Primary

MeasureTime frame
Symptomatic relief from cyclical mastalgia.Timepoint: Outcome will be assessed at 4,8,12 and 24 weeks

Secondary

MeasureTime frame
Improvement in fibroadenosis as well as reduction in size of fibroadenoma.Timepoint: Outcome will be assessed at 4,8,12 & 24 weeks

Countries

India

Contacts

Public ContactDharmendra Tarkar

UPUMS SAIFAI ETAWAH

somendrachauhan@hotmail.com7906265532

Outcome results

None listed

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