To see how homoeopathic treatment works in women with depression and breastfeeding problems after pregnancy

Efficacy of individualized homoeopathic management in cases of postpartum depression and lactation failure with validated clinical and psychiatric assessment A single arm clinical trail - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/01/102377

Enrollment

Registered

2026-01-28

Start date

Unknown

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

Health Condition 1: O924- Hypogalactia Health Condition 2: F39- Unspecified mood [affective] disorder

Interventions

Intervention1: Homoeopathic Management: Individualized homoeopathic medicine prescribed based on detailed case taking and repertorization. Homoeopathic medicine will be selected according to the total

Eligibility

Inclusion criteria

Inclusion criteria: Age Women aged between 18 to 35 years Postpartum Status from delivery of baby till 1 year from that period Parity Both primipara and multiparous women Presence of at least one postpartum health disorder under the study scope Clinically stable and not requiring emergency medical or surgical intervention Willing and able to provide written consent Ability to understand and respond study language (regional or English ) Willing to adhere to the follow up schedule and assessments throughout the study period

Exclusion criteria

Exclusion criteria: Grand multipara (5 or more viable births) HIV positive women Severe or emergency conditions requiring immediate attention such as PPH puerperal pyrexia breast abscess puerperal psychosis and very strong suicidal inclination Uncontrolled chronic illnesses such as diabetes, hypertension (eclampsia) renal disease, epilepsy or thyroid dysfunction that may confound outcomes Unwilling to participate in study or already a part of another study Inability to understand or communicate in the study language (local language or English) affecting assessment accuracy

Design outcomes

Primary

Measure	Time frame
Outcome assessment will be done by applying EPDS Edinburgh postpartum depression scale and LATCH scale before and after intervention Timepoint: Baseline (pre study) at 0 days EPDS Edinburgh postpartum depression scale and LATCH scale will be applied to asses score Mid study (follow up) will be taken every 15 days Post study at the end of 3rd month again EPDS Edinburgh postpartum depression scale and LATCH scale will be applied to asses post study score	—

Measure

Time frame

Outcome assessment will be done by applying EPDS Edinburgh postpartum depression scale and LATCH scale before and after intervention Timepoint: Baseline (pre study) at 0 days EPDS Edinburgh postpartum depression scale and LATCH scale will be applied to asses score Mid study (follow up) will be taken every 15 days Post study at the end of 3rd month again EPDS Edinburgh postpartum depression scale and LATCH scale will be applied to asses post study score

—

Secondary

Measure	Time frame
NILTimepoint: NIL	—

Countries

India

Contacts

Public ContactDr Manasi Waman Patwardhan

Dr J J Magdum Homoeopathic Medical College

pawarpadmashree1@gmail.com9975377151

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026