None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Married pregnant women aged 21 to 35 years who are willing and able to participate in the study will be included. Participants must have no previous history of pregnancies affected by chromosomal defects. They should have a hemoglobin level greater than 9 g/dL and blood pressure within the range of 110/70 mmHg to 130/90 mmHg (not exceeding this range) Additionally, the patients should be experiencing mild to moderate associated symptoms of pregnancy
Exclusion criteria
Exclusion criteria: Patients who are not willing or able to participate in the study will be excluded. Those with high-risk pregnancies will also be excluded. This includes patients presenting with conditions such as hyperemesis gravidarum, pre-eclampsia, gestational diabetes mellitus, intrauterine growth restriction (IUGR), intrauterine death (IUD), thyroid dysfunction, or any other significant pregnancy-related complications.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Give a relief in some symptoms of normal pregnancy generalized weakness morning sickness tiredness anorexia nausea vomiting etc to the patient in 3 monthsTimepoint: Give a relief in some symptoms of normal pregnancy generalized weakness morning sickness tiredness anorexia nausea vomiting etc to the patient in 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Releif in the symptoms like nausea vomiting morning sickness anorexia genral debility mood swings etcTimepoint: 3 months | — |
Countries
India
Contacts
Govt ayurvedic medical college and hospital chaukaghat varansi