None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The study will include married pregnant women between the ages of 21 and 35 who voluntarily consent to participate. Eligibility criteria require that participants have no history of previous abnormal pregnancies or pregnancies affected by chromosomal abnormalities. Additionally, they must have a hemoglobin (Hb) level of more than 9 g/dl and a blood pressure range between 100/60 mmHg and 130/90 mmHg. Only women presenting with mild to moderate pregnancy symptoms will be considered for inclusion
Exclusion criteria
Exclusion criteria: Patients with high-risk pregnancies, hyperemesis gravidarum, pre-eclampsiagestational diabetes, IUGR, IUD, thyroid malfunction, and other conditions are not willing or able to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Give a relief in some symptoms of normal pregnancy like generalised weakness, tiredness, morning sickness anorexia, nausea, vomiting etc. to the patient.Timepoint: 9 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Relief in the symptoms like nausea and vomiting, morning sickness, anorexia, general debility, mood swings, etc.Timepoint: 9 months | — |
Countries
India
Contacts
Government PG Ayurveda College and Hospital