CTRI/2013/04/003542
Active, not recruiting
未知
A Cross-sectional, Multicentre, Out â?? patient clinic based study to determine the prevalence of recurrent spontaneous miscarriages among Indian women with a history of at least one miscarriage
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Abbott India Limited
- Enrollment
- 750
- Status
- Active, not recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Female patients aged between 18 to 45 years, both inclusive
- •2\.History of at least one spontaneous miscarriage of \<\= 20 weeks gestation
- •3\.Willing to provide written Patient Authorization.
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
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
Survey to understand the demographics, diagnosis, clinical presentation in patients with acid peptic diseaseCTRI/2021/02/031271Dr Reddys Laboratories Ltd3,739
Recruiting
Not Applicable
To aim of this study is to determine the prevalence of Non-Alcoholic Fatty Liver Disease and Thyroid Dysfunction in Patients with Metabolic Syndrome.Health Condition 1: null- Patients with an established diagnosis of MetS as per the ATP III criteria and visiting the clinic as a part of their scheduleCTRI/2016/09/007270Abbott India Limited400
Active, not recruiting
Not Applicable
A multicenter, randomized, parallel patients’ group, comparative clinical trial for the assessement of efficacy and safety of Pelethrocin®/HELP 500 mg (generic diosmin & hesperidin MPFF) versus Daflon®/Servier 500 mg (original diosmin & hesperidin MPFF) in the treatment of chronic venous insufficiency patients (a therapeutic equivalence trial).Chronic Venous InsufficiencyMedDRA version: 9.1Level: LLTClassification code 10066682Term: Chronic venous insufficiencyEUCTR2007-001947-23-GRHELP Pharmaceuticals S.A.
Suspended
Not Applicable
Evaluating the effects of high and low oxygen therapy compared to standard oxygen therapy in patients undergoing major surgery under general anaesthesiaHyperoxia, hyperoxaemiaMajor non-cardiac surgerySurgical site infectionPostoperative complicationsAnaesthesiology - AnaestheticsACTRN12619000115134Medical Research Institute of New Zealand2,640
Active, not recruiting
Not Applicable
A Multicenter, Randomized, Comparative, Patient-blinded Study to Evaluate the Safety and Efficacy of G-CSF Alone Versus AMD3100 (240 µg/kg) Added to a G-CSF Mobilization Regimen in Adult Patients with Non-Hodgkin’s Lymphoma (NHL), Hodgkin’s Disease (HD) or Multiple Myeloma (MM) Who Have Previously Failed Stem Cell Collections.EUCTR2006-004247-29-DEGenzyme Europe BV