Perfusion Index and Labor Analgesia

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-05-30

Study Completion Date

2017-08-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

It can be suggested that sympathetic tonus increase and pain, caused by the removal of the effect of epidural analgesia applied at birth, may also affect perfüsion index. The purpose of this study is; To correlate the VAS value at the time of return of epidural analgesia with the PI values at that time and, to test the possibility of using PI variants as an objective tool for predicting pain initiation time and assessing pain.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

The Effect of Wireless Electronic Fetal Monitoring on Labor Pain and Birth Experiences

NCT07233187

Birth Intrapartum

NOT_YET_RECRUITING NA

The Effects of Epidural Analgesia on Maternal-Infant Bonding and Birth-Related Trauma

NCT07077785

Epidural Anesthesia in Labor and Delivery

NOT_YET_RECRUITING NA

The Effect of Foot Reflexology Massage on the Perception of Labor Pain in Nulliparous Pregnant Women

NCT07045675

Massage Labor Pain Foot Massage +1 more

ACTIVE_NOT_RECRUITING

Perineal Massage and Warm Application in Labor

NCT06005077

Perineal Injury Pain Labor

COMPLETED NA

The Effect of the Intrapartum Care Model Given in Line With WHO Recommendations on the Birth Process and Care

NCT06681675

Birth Outcomes Labor Pain and to Reduce Pain Fear of Birth +5 more

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

perfüsion Index in Removal of the Epidural Analgesia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

perfüsion index

Determination of the relationship between VAS values and PI in patients with normal delivery who undergo epidural analgesia

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* women who will give normal spontaneous vaginal delivery
* Between the ages of 18-45

Exclusion Criteria

* Patients who do not accept the procedure,
* those under 18 years of age - over 45 years,
* those with low platelet counts,
* those with infection at the puncture site,
* those with progressive neurological disease,
* Those with increased intracranial pressure,
* those with hypovolemia

Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No