Diagnostic Accuracy of 10-Minute Vs 30-Minute CTG in intrapartum fetal monitoring.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR202512844760265

Enrollment

200

Registered

2025-12-03

Start date

2025-12-12

Completion date

Unknown

Last updated

2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fertility-female Paediatrics

Interventions

CTG 10min

CTG 30min

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: • Singleton pregnancy. • Gestational age = 37 weeks. • Vertex presentation. • Active first stage of labor (cervical dilation = 4 cm). • Low-risk pregnancy (no hypertension, diabetes, IUGR, or other significant complications).

Exclusion criteria

Exclusion criteria: • Multiple gestation. • Known major fetal anomaly. • Non-vertex presentation. • Indication for continuous CTG (e.g., meconium-stained liquor, antepartum hemorrhage). • Maternal refusal

Design outcomes

Primary

Measure	Time frame
To compare the diagnostic accuracy (sensitivity, specificity, PPV, NPV) of a 10 minute CTG versus a standard 30-minute CTG in detecting fetal acidaemia defined as (umbilical venous pH < 7.25).	—

Secondary

Measure	Time frame
• To compare the average monitoring time required for each protocol. • Neonatal outcomes (Apgar score, NICU admission) • To measure healthcare provider satisfaction with shortened CTG	—

Countries

Egypt

Contacts

Public ContactElwani Elderemy;Seif ElEsalm ElSenousi Fas;Ahmed Ali

proffesor;Doctor

alwany.elsenousy@med.aun.edu.eg;Seifali-2020@aun.edu.eg01225005036;01004971596

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026