Evaluation Of The Efficacy Of Shatapushpa Taila Nasya In The Management Of Artava Kshaya

Evaluation of the efficacy of shatapushpa taila nasya in the management of artava kshaya

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/06/053524

Enrollment

Registered

2023-06-05

Start date

Unknown

Completion date

Unknown

Last updated

2023-06-26

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

Conditions

Health Condition 1: N915- Oligomenorrhea, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Infrequent Menses At Interval Between Two Cycle Exceeding More Than 35 Days 2. Reduced Quantity Of Flow That Is Using Less Than 2 Pads Per Day 3.Artava Kshaya Due To PCOD 4.Duration Of Flow Less Than Two Days 5.Irrespective Of Marriage

Exclusion criteria

Exclusion criteria: Pregnant Women Lactating Women Patient Having Systemic Disorders Hyperthyroidism Severe Anaemia hb level Less Than 7Gm/Dl Any Type Of Malignancy.

Design outcomes

Primary

Measure	Time frame
Decrease In Symptoms Of Artava Kshaya Like Normalise The Interval Between Two Cycles To Normalise The Amount Of Blood Loss To Normalise The Duration Of Bleeding MInimise The Grade Of PainTimepoint: 3 months	—

Secondary

Measure	Time frame
Ultrasonography of lower abdomen to be within normal limit TSH T3 T4 Serum prolactin HaemoglobinTimepoint: 90 Days	—

Countries

India

Contacts

Public ContactDr Dipak Kumar Goswami

Govt Ayurvedic College And Hospital

dr.dkgoswami@gmail.com8486324789

Outcome results