Evaluation of Management and Outcomes of Normal Labor in Eldakhla Hospital

April 3, 2025 updated by: Dina Abdel Baset Ahmed, Assiut University

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

Not yet recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

176

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

May 1, 2025

Primary Completion (Estimated)

May 1, 2026

Study Completion (Estimated)

August 1, 2027

Study Registration Dates

First Submitted

April 3, 2025

First Submitted That Met QC Criteria

April 3, 2025

First Posted (Actual)

April 10, 2025

Study Record Updates

Last Update Posted (Actual)

April 10, 2025

Last Update Submitted That Met QC Criteria

April 3, 2025

Last Verified

April 1, 2025

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

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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