Overview

N-Acetyl Cysteine for Prevention of Preterm Birth

Status:
Completed
Trial end date:
2007-12-01
Target enrollment:
0
Participant gender:
Female
Summary
The antioxidant effect of N-Acetyl cysteine can abort the inflammatory cascade responsible for initiation of preterm labour especially among patients with reccurent preterm birth and patients having bacterial vaginosis
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Assiut University
Treatments:
Acetylcysteine
N-monoacetylcystine
Progesterone
Criteria
Inclusion Criteria:

- Patients with previous preterm labour who attended the antenatal care clinic at Assiut
University Hospital were recruited and counseled about participating in the study.

- A written informed consent was taken.

- Patients had the right to refuse to participate and/or withdraw from the study at ay
time without being denied their regular full clinical care.

- Personal information as well as data collected were subjected to confidentiality and
were not made available to third party.

Exclusion Criteria:

- Patients were excluded if they refused to participate in the study, had prelabour
premature rupture of membranes (PPROM), had an incompetent cervical os proved by
funneling of the internal os on ultrasound examination or by a documented history with
or without a cercelage done in the previous or current pregnancy.

- Patients with twin pregnancy, intrauterine foetal death, malpresentations, known fetal
anomaly, progesterone or heparin treatment during the current pregnancy, hypertension
requiring medication, a seizure disorder, Irregular and/or unsure menstrual dates or
abortion within 3 months prior to the last menses were also excluded.