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A clinical trial to study the effect of rajaswala paricharya in patients with premenstrual syndrome

A randomized open labelled controlled clinical study to evaluate the effect of rajaswala paricharya in the management of premenstrual syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/049344
Enrollment
40
Registered
2023-01-31
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: N943- Premenstrual tension syndrome

Interventions

None listed

Sponsors

Sri Sri College of Ayurvedic Science and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects presenting symptoms of premenstrual syndrome (PMS). 2.Subjects who are willing to give written consent for the study.

Exclusion criteria

Exclusion criteria: 1.Subjects with irregular menstruation. 2.Subjects undergoing any pharmacologic therapy, hormone ingestion or alcohol use 3.Subjects exhibiting symptoms continues throughout the phase of menstrual cycle. 4.Subjects with underlying pathological conditions of breast and pelvis. 5. Known cases of Hypo/hyperthyroidism, anemia. 6. Subjects with Premenstrual Dysmorphic Disorder (PMDD) and any pre-existing psychological disorder.

Design outcomes

Primary

MeasureTime frame
1. Record of Severity of Problems (DRSP) Symptom Diary. 2. Premenstrual Tension Syndrome Rating Scale (PMTS-OR)Timepoint: 3 months—

Secondary

MeasureTime frame
1. Number of subjects following each regime in every month 2.To study the principles behind Rajaswala Paricharya and its application in today’s lifestyle. Timepoint: 3 months—

Countries

India

Contacts

Public ContactPREETHA S

Sri Sri College of Ayurvedic Science and Research

sharon.avp@gmail.com9884832050

Outcome results

None listed

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