Unknown PHASE4 INTERVENTIONAL 1-arm NCT03164096

The Effect of Some Parturients' Characteristics on Sensory Block Level After Spinal Anesthesia

The Effect of Body Mass Index, Intra-abdominal Pressure, Abdominal Girth and Waist Circumference on Sensory Block Level After Single-shot Spinal Anesthesia for Cesarean Section

Sponsor: Assiut University

Conditions Anesthesia, Obstetrical

Interventions Bupivacaine Hydrochloride

Updated 8 times since 2017 Last updated: Mar 28, 2018 Started: Jun 1, 2017 Primary completion: Dec 1, 2018 Completion: Dec 10, 2018

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Listed as NCT03164096, this PHASE4 trial focuses on Anesthesia, Obstetrical and remains ongoing. Sponsored by Assiut University, it has been updated 8 times since 2017, reflecting limited change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.

Status Flow

Change History

8 versions recorded

Sep 2025 — Present [monthly]

Unknown PHASE4
Sep 2024 — Sep 2025 [monthly]

Unknown PHASE4
Jul 2024 — Sep 2024 [monthly]

Unknown PHASE4

Status: Unknown Status → Unknown
Jan 2021 — Jul 2024 [monthly]

Unknown Status PHASE4
Feb 2020 — Jan 2021 [monthly]

Unknown Status PHASE4

Status: Recruiting → Unknown Status

▶ Show 3 earlier versions

Jun 2018 — Feb 2020 [monthly]

Recruiting PHASE4
Aug 2017 — Jun 2018 [monthly]

Recruiting PHASE4

Status: Not Yet Recruiting → Recruiting
Jun 2017 — Aug 2017 [monthly]

Not Yet Recruiting PHASE4

First recorded

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Assiut University

Data source: Assiut University

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

• Asyut, Egypt