CClinicalTrials.gg
Status unknownNCT04617249Updated Nov 5, 2020

Median and Paramedian Anesthesia in Cesarean Section

An interventional study of median anesthesia and paramedian anesthesia in Anesthesia, sponsored by Aljazeera Hospital. Status unknown at 1 site in Egypt. Open to female participants aged 18 Years to 42 Years. Per ClinicalTrials.gov, last updated 2020-11-05.

Sponsored by Aljazeera Hospital · Not applicable, Interventional, and Other

The sponsor has not verified this record recently (last verified Oct 2020), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years to 42 Years
Sex
Female
01

Study summary

The number of cesarean sections worldwide has markedly been increasing since 1985.Intrathecal anesthesia is preferred by most anesthesiologists over general anesthesia

Read the detailed description

Complications with spinal anesthesia are not common which makes it difficult to detect its incidence and one of the most serious complications is nerve injury.

02

Conditions studied

  • Anesthesia
03

In context

Lead sponsor

Aljazeera Hospital is the lead sponsor of 63 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 42 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Age 18-42 years
  • Scheduled for elective cesarean section
  • ASA II

Exclusion criteria

Exclusion Criteria:

  • -Age \<18 years or >42 years
  • ASA >II
  • Emergency cesarean section
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
80 participants (estimated)

Study arms

  • Active comparator
    Giving median anesthesia

    Procedure: median anesthesia

  • Active comparator
    Giving paramedian anesthesia

    Procedure: paramedian anesthesia

Interventions

  • Proceduremedian anesthesia

    giving median anesthesia

  • Procedureparamedian anesthesia

    giving paramedian anesthesia

06

What researchers measure

Primary outcomes

  1. the number of women who will have less pain

    the number of women who will have less pain post procedure

    Time frame: 3 days

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Study locations

1 site
  • Aljazeera( Al Gazeera) hospital
    Giza, Egypt
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 5, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04617249
Lead sponsor
Aljazeera Hospital
Responsible party
Sponsor
First posted
Nov 5, 2020
Start date
Nov 5, 2020 (estimated)
Primary completion
Apr 25, 2021 (estimated)
Completion
May 15, 2021 (estimated)
Last update
Nov 5, 2020

Study contacts

Mahmoud Alalfy
Contact
mahmoudalalfy@ymail.com
01002611058
Mahmoud Alalfy
study chair · Algezeera hospitaland National Research Centre ,Egypt

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2020. You cannot join it, but the record below documents what was studied.

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