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Centchroman vs tamoxifen in patients with breast pai

Not Applicable
Conditions
Health Condition 1: N644- Mastodynia
Registration Number
CTRI/2023/11/059992
Lead Sponsor
on-funded
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. All female patients, aged >18 years

2. Patients, who have complain of mastalgia with or without breast fibroadenoma having persistent symptoms for more than 1 month after reassurance and supportive breast management.

3. Pain severity of >3/10 on visual analog scale.

Exclusion Criteria

1. Acute inflammatory breast conditions (cellulitis , breast abscess)

2. suspicion of malignancy ( clinical or radiological)

3. Family history of breast and ovarian carcinoma

4. Contraindication to centchroman and tamoxifen —--

a.Pregnancy

b.Polycystic ovarian diseases ( PCOD )

c.Cervical hyperplasia do

d.Recent history or clinical evidence of jaundice or liver diseases

e Conditions like, chronic illness such as tuberculosis, renal diseases, severe allergic states etc.

f.Patients willing to conceive within six months.

5.History of chest trauma

6.Severe drug reaction to either centchroman or tamoxifen after starting treatment

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The comparison of pain score in the mastalgia patients with or without fibroadenoma undergoing treatment with centchroman and tamoxifen with Visual analog scale at end of 3 month treatment. <br/ ><br>Timepoint: Visual analog scale at end of 3 month treatment. <br/ ><br> <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
To compare the response in size of fibroadenoma <br/ ><br>To compare patient satisfaction with likert scale <br/ ><br>Timepoint: Visual analog scale at end of 3 month treatment. <br/ ><br>
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