Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Subject(Pregnant women ) who will give consent for trial. Primigravida, Primipara and Multigravida Normal range of haematological/routine ANC investigation Subject having gynecoid pelvis,borderline pelvis and cephalic presentation Mild preeclampsia
Exclusion criteria
Exclusion criteria: Subject(Pregnant Women)not willing to trial Multipara CPD Subject (Pregnant women)having mal-presentation APH Subject(Pregnant women) having Hb less than 8gm% Moderate to severe Pre-eclampsia Subject (Pregnant women )having any associated gynaecological conditions or systemic disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Spontaneous onset of labor and normal Progress of laborTimepoint: 34 weeks of gestation to till delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| The Clinical result will be assessed by observing the progress of Labor Any associated Complaints during trial period will be recordedTimepoint: From 34 weeks of gestation till delivery | — |
Countries
India
Contacts
Rajiv Gandhi Government Postgraduate Ayurvedic College and Hospital Kangra Paprola