- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06922435
Evaluation of Management and Outcomes of Normal Labor in Eldakhla Hospital
Evaluation of Management and Outcomes of Normal Labor in Eldakhla Hospital.
Labour is a physiologic process during which the products of conception are expelled outside of the uterus. Labour is achieved with changes in the biochemical connective tissue and with gradual effacement and dilatation of the uterine cervix as a result of rhythmic uterine contractions of sufficient frequency, intensity, and duration The WHO definition further stated that the aim of care in normal birth is to achieve a healthy mother and child with the least possible level of interventions, and in every case, there should be a valid reason to interfere with the natural process.
The presence of changes in cervical effacement, dilation, position, consistency, and descent of the presenting part are the key indicators in identifying the stages of labour. Concomitant with the increased frequency of contractions, a patient perceives the descent of the fetus into her pelvis as lightening (3).
The process from the 1st to the 3rd stage is a continuum without any break. The first stage of labour is the beginning and longest stage and largely determines the outcome of the labour process because commonly, a normal first stage is followed by a normal 2nd and 3rd stages of labour. Hence, in current clinical practice, the management of labour virtually equates to the management of the first stage. The pain associated with labour is a unique and complex phenomenon. Whilst typical experiences of pain tend to be associated with injury or disease, labour pain emerges during a vital and highly positive event. In fact, as the pain intensity rises, the labour is seen to be progressing normally.
The clinical audit is the systematic and critical analysis of the quality of medical care, including the procedures used for diagnosis and treatment, the use of resources and the resulting outcome and quality of life for the patient.
Reviewing of care included three domains "structure, process and outcomes" which are selected and evaluated in a systematic way according to explicit criteria .
This definition highlights two key features of the process of audit. First, audit involves a criticism of current practice. Second audit is not restricted to the technical accuracy of diagnosis or treatment but also involves diverse issues such as for example the timeliness of interventions, the appropriateness of referral, the attitudes of staff or the information given to the patient the aim of the study To improve service and quality for patients of the normal labour in the department of Obstetrics and Gynecology, Dakhla Hospital.
To assess and evaluate the practices, procedures, and outcomes of normal labor.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Patients with full-term labour that included all women who will be fullfilling the following criteria:
- Age from 18 -40 years,
- gestational age: complete 37 weeks gestation-41ws+6 days,
- True labour pain associated with cervical changes, Cervical dilation > 3 cm
Description
Inclusion Criteria:
Patients with full-term labour that included all women who will be fullfilling the following criteria:
- Age from 18 -40 years,
- gestational age: complete 37 weeks gestation-41ws+6 days,
- True labour pain associated with cervical changes, Cervical dilation > 3 cm
Exclusion Criteria:
- Multiple gestations, Fetal malformations, Complicated pregnancy (hypertension, diabetes. etc...), Intrauterine growth restriction or macrosomic fetuses, Antepartum hemorrhage or presence of meconium-stained fluid, Preterm labour and false labour pain.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Group A
Patients with full-term labour
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maternal outcomes
Time Frame: 7 days
|
post-partum hemorrhage percentage
|
7 days
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- M &O normal labor Eldakhla
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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