The Association Between Parathyroid Hormone and Preterm Labor

Sponsor
Ain Shams Maternity Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT05688007
Collaborator
(none)
100
1
21
4.8

Study Details

Study Description

Brief Summary

This observational study aims to test the level of parathyroid hormone in pregnant women. The main question it aims to answer is:

n Pregnant women, are the levels of serum PTH, calcium, magnesium, phosphorus & albumin similar in both preterm and term births?

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: parathyroid hormone level
  • Diagnostic Test: serum electrolytes

Detailed Description

  • Approval from ethical committee will be sought.

  • 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  • Venous blood samples will be withdrawn about (3ml) once from every patient within one hour from inclusion into the study to measure serum parathyroid hormone, calcium, magnesium, phosphorus and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.

Study Design

Study Type:
Observational
Actual Enrollment :
100 participants
Observational Model:
Case-Control
Time Perspective:
Cross-Sectional
Official Title:
The Association Between Parathyroid Hormone and Preterm Labor
Actual Study Start Date :
Apr 1, 2021
Actual Primary Completion Date :
Oct 16, 2022
Actual Study Completion Date :
Dec 30, 2022

Arms and Interventions

Arm Intervention/Treatment
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).

Diagnostic Test: parathyroid hormone level
Serum level of parathyroid hormone

Diagnostic Test: serum electrolytes
Serum levels of: magnesium, phosphorus, calcium, and albumin

Controls

pregnant women not in labor - gestational age: (28- 36 weeks)

Diagnostic Test: parathyroid hormone level
Serum level of parathyroid hormone

Diagnostic Test: serum electrolytes
Serum levels of: magnesium, phosphorus, calcium, and albumin

Outcome Measures

Primary Outcome Measures

  1. parathyroid hormone [1 day]

    serum level of parathyroid hormone (ng/L)

Secondary Outcome Measures

  1. Calcium [1 day]

    serum calcium level (mg/dl)

  2. Magnesium [1 day]

    serum magnesium level (meq/L)

  3. Phosphorus [1 day]

    serum phosphorus level (mg/dl)

  4. Albumin [1 day]

    serum albumin level (g/dl)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Pregnant women aged (18-40).

  • Gestational age (28-36 weeks).

Exclusion Criteria:
  • Known maternal disease as diabetes, hypertension, renal disease, cardiac disease and liver disease.

  • Known hypo or hyperparathyroidism

  • Multiple pregnancy

  • Polyhydramnios

  • Premature rupture of membrane

  • Antepartum Hemorrhage

  • Uterine malformations e.g. bicornuate uterus

  • Smoking

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ain Shams Maternity Hospital Cairo Egypt

Sponsors and Collaborators

  • Ain Shams Maternity Hospital

Investigators

  • Study Director: Sherif A Ashoush, MD, Faculty of Medicine Ain Shams University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Rania Hassan Mostafa, Principal Investigator, Ain Shams Maternity Hospital
ClinicalTrials.gov Identifier:
NCT05688007
Other Study ID Numbers:
  • MS 168/2021
First Posted:
Jan 18, 2023
Last Update Posted:
Jan 18, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Rania Hassan Mostafa, Principal Investigator, Ain Shams Maternity Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 18, 2023