The Association Between Parathyroid Hormone and Preterm Labor
NCT ID: NCT05688007
Last Updated: 2023-01-18
Study Results
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.
COMPLETED
100 participants
OBSERVATIONAL
2021-04-01
2022-12-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
n Pregnant women, are the levels of serum PTH, calcium, magnesium, phosphorus \& albumin similar in both preterm and term births?
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Bone Health in Hyperemesis Gravidarum
NCT02862496
Androgens Level in the Third Trimester of Pregnancy in Patients With Preeclampsia
NCT02992145
Low Dose Calcium to Prevent Preeclampsia
NCT02338687
Vitamin D Treatment and Hypocalcemic Pregnant Women
NCT02021864
Maternal Serum Amyloid A Levels in Pregnancies Complicated With Preterm Labour.
NCT03205020
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
* Patients will be enrolled from Ain Shams University Maternity Hospital labor ward and antenatal outpatient clinic.
* History, examination and fetal ultrasound will be done to identify eligible patients.
History: a full detailed history including personal, menstrual, obstetric, present, past history and family history will be obtained.
Accurate last menstrual period date will be obtained, and gestational age will be calculated using Naegele's rule or first trimester ultrasound to identify preterm patients with gestational age (28-36 weeks).
Examination: general, abdominal and vaginal examination to identify patients in established labor with Regular uterine contractions are at least 3 in 10 min each lasting 40 seconds. Progressive cervical dilatation (at least 4 cm). Ultrasound: for (viability of fetus, fetal biometry and estimated fetal weight, amniotic fluid, placental localization).
Thus, two groups of patients will be identified:
1. Cases: established preterm labor - gestational age: (28-36 weeks)
2. Controls: pregnant women not in labor - gestational age: (28- 36 weeks)
* Venous blood samples will be withdrawn about (3ml) once from every patient within one hour from inclusion into the study to measure serum parathyroid hormone, calcium, magnesium, phosphorus and albumin levels.
* Samples will not be collected from an arm with an intravenous catheter if alternate sites are available.
* Patient collection site will be appropriately disinfected prior to sample collection.
* After collection, samples will be put in a red or yellow tube (serum separating tube) with a serum gel separator.
* Samples will be gently mixed immediately following collection into tube to ensure proper preservation of the analytes. 180° tube inversion, allowing bubble to travel the length of the tube, followed by return to upright position is one mix.
* Samples will be delivered to laboratory within 30 to 60 minutes.
* Data will be collected and recorded in a case report form (Age, parity, previous preterm births/ miscarriage, gestational age, measured levels of serum PTH, calcium, magnesium, phosphorus \& albumin , mode of delivery, birth weight).
* Statistical analysis will be done to get results.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Cases
pregnant women with established preterm labor - gestational age: (28-36 weeks), having: Regular uterine contractions are at least 3 in 10 min each lasting 40 seconds. Progressive cervical dilatation (at least 4 cm).
parathyroid hormone level
Serum level of parathyroid hormone
serum electrolytes
Serum levels of: magnesium, phosphorus, calcium, and albumin
Controls
pregnant women not in labor - gestational age: (28- 36 weeks)
parathyroid hormone level
Serum level of parathyroid hormone
serum electrolytes
Serum levels of: magnesium, phosphorus, calcium, and albumin
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
parathyroid hormone level
Serum level of parathyroid hormone
serum electrolytes
Serum levels of: magnesium, phosphorus, calcium, and albumin
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Gestational age (28-36 weeks).
Exclusion Criteria
* Known hypo or hyperparathyroidism
* Multiple pregnancy
* Polyhydramnios
* Premature rupture of membrane
* Antepartum Hemorrhage
* Uterine malformations e.g. bicornuate uterus
* Smoking
18 Years
40 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ain Shams Maternity Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Rania Hassan Mostafa
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Sherif A Ashoush, MD
Role: STUDY_DIRECTOR
Faculty of Medicine Ain Shams University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ain Shams Maternity Hospital
Cairo, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
MS 168/2021
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.