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A study to determine the yakkai ilakkanam in abnormal uterine bleeding patients attending OPD National Institute of Siddha

An observational study to determine the possible association between specific yakkai ilakkanam (Siddha somatotype) in patients with Abnormal uterine bleeding Perumbadu - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/05/067959
Enrollment
220
Registered
2024-05-27
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: N926- Irregular menstruation, unspecified

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subject is assessed with PBAC for abnormal uterine bleeding with the following conditions- Fibroid uterus, Adenomyosis, Pelvic endometriosis, Dysfunctional uterine bleeding, Chronic tubo ovarian mass, Endocrinal - hypothyroid and hyperthyroid, Hematological cause and are included in the study

Exclusion criteria

Exclusion criteria: Patient not willing to sign the consent form Patients with any serious system illness Metrorrhagia

Design outcomes

Primary

MeasureTime frame
The possible association of Dhegi characterization in Perumbadu patients will be obtained.Timepoint: 18 months—

Secondary

MeasureTime frame
The Naadi in the subjects of the study will be documented. The affected humors in the subjects will be evaluated through the panchapatchi calculation. Timepoint: 18 months—

Countries

India

Contacts

Public ContactDr V Srinivasan

National Institute of Siddha

seenunis47@gmail.com9965962592

Outcome results

None listed

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