clinical study on shatpushpa taila nasya(nasal drops) in absence of menses .

Effect of Shatpushpa taila Navana nasya in Artavakshaya for varying durations- A randomized controlled clinical trial - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/04/066520

Enrollment

Registered

2024-04-30

Start date

Unknown

Completion date

Unknown

Last updated

2024-05-27

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: a.)Female patients between the age of 18-35 yrs. b.)Amenorrhea beyond 6 weeks c.) Individual who provide informed consent prior to treatment and voluntarily participate in the trial

Exclusion criteria

Exclusion criteria: a.)Pregnancy b.)Lactating mother c.)Primary amenorrhea d.)Chronic systemic illness e.)Premature menopause f.)Contraindication of navan nasya(navana nasya)

Design outcomes

Primary

Measure	Time frame
Onset of menstruationTimepoint: 14days	—

Secondary

Measure	Time frame
Compare effect of Navan Nasya given for 3 days, 5 days and 7 daysTimepoint: 14days	—

Countries

India

Contacts

Public ContactProf Dr Sujata Kadam

All India Institute of Ayurveda

sujatadkadam@gmail.com9890305370

Outcome results