Role of Serum Total Antioxidant Level in Preterm Labor

Ain Shams Maternity Hospital

Status: Unknown

Conditions: Preterm Labor

Study type: Observational

Funder types: Other

Identifiers

NCT01518816

ABDO-0100

Details and patient eligibility

About

The aim of this study is to detect the association between maternal serum antioxidant level and preterm labor.

Full description

Study design:

This is a prospective case-control study.

Setting:

The study will be conducted at Ain Shams University Maternity Hospital.

Population of the study:

A total of 70 pregnant women attending the outpatient obstetric clinic and inpatient of Obstetrics and Gynecology department or when they will be admitted to the delivary room of Ain Shams university hospital.

Patient will be divided in to two groups. Group A: 35 pregnant women diagnosed with preterm labor(Preterm labor pain at least 3 contraction every 20 minutes ,cervical dilatation < 2cm and effacement< 50%) which will deliver within one week maximum after hospitalization.

Group B: 35 pregnant women( controls )with uncomplicated pregnancies at a similar gestational ages followed routinely in the antenatal care unit.

Every case will be subjected to:-

1. Written informed consent before the study.
2. Complete history .
3. Complete general and abdominal examination.
4. Infection markers(CRP,WBCs count, urine analysis ).
5. Gestational age determination by the last menstrual date or Ultrasonography.
6. Local pelvic examination.

Enrollment: 70 estimated patients

Sex: Female

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Preterm labor(pregnant between 28th and 37th week).
• Singleton pregnancy.
• Amnion membranes were intact

Exclusion criteria

• Past history of preterm labor or premature delivery.
• Urinary tract infections and any other infections.
• Poly- or oligohydramnios.
• Fetal distress, fetal or uterine anomaly.
• Membranes rupture and placenta pathology.
• Preeclampsia or intrauterine growth retardation

Trial design

70 participants in 2 patient groups

preterm labor cases

Description:

Group A: 35 pregnant women diagnosed with preterm labor(Preterm labor pain at least 3 contraction every 20 minutes ,cervical dilatation \< 2cm and effacement\< 50%) which will deliver within one week maximum after hospitalization.

control group

Description:

Group B: 35 pregnant women( controls )with uncomplicated pregnancies at a similar gestational ages followed routinely in the antenatal care unit.