None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Female patients aged between 18 to 45 years, both inclusive 2.History of at least one spontaneous miscarriage of 3.Willing to provide written Patient Authorization.
Exclusion criteria
Exclusion criteria: 1.Female patients unable to provide written authorization 2.Any condition that in the opinion of the investigator, does not justify the patients inclusion in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary Objective: Prevalence (%) of female patients with recurrent spontaneous miscarriagesTimepoint: Its a epidemiology study. Patient will come at the site only once. Hence there is only one visit. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)To compare the age-specific miscarriages in patients with 3 and â?¥ 3 spontaneous miscarriages of â?¤ 20 weeks gestation 2)To determine the percentage (%) of patients with associated risk factors having recurrent spontaneous miscarriages (defined as â?¥ 3 pregnancy losses of â?¤ 20 weeks gestation) in comparison to those with no risk factors Timepoint: Outcome conti.. 3)To determine the probability of a subsequent miscarriage after the first miscarriage 4)To determine any correlation between recurrent spontaneous miscarriages (defined as â?¥ 3 pregnancy losses of â?¤ 20 weeks gestation) and associated risk factors | — |
Countries
India