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Sharp Versus Blunt Uterine Incision Expansion

Comparison Between Blunt Versus Sharp Expansion of Uterine Incision at Lower Segment Cesarean Section as Regards the Intra-operative Blood Loss & Postoperative Pain

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03377894
Enrollment
200
Registered
2017-12-19
Start date
2017-12-31
Completion date
2018-03-31
Last updated
2017-12-19

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

Conditions

Cesarean Section Complications

Brief summary

comparison between blunt versus sharp expansion of uterine incision at lower segment cesarean section in primigravida as regards the intra-operative blood loss & postoperative pain

Detailed description

the study includes 200 pregnant women, primigravidas, at term who underwent elective transverse lower segment Cesarean section for the first time among the age group of 20 - 37 years with a singleton pregnancy. The patients are divided randomly into two groups as follows: * Group (A): undergoing blunt uterine incision expansion * Group (B): undergoing sharp uterine incision expansion

Interventions

PROCEDUREblunt uterine incision expansion

blunt uterine incision expansion

PROCEDUREsharp uterine incision expansion

sharp uterine incision expansion

Sponsors

Kasr El Aini Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 37 Years
Healthy volunteers
No

Inclusion criteria

* singleton pregnancy.

Exclusion criteria

* previous PID * any medical or psychiatric * patients with BMI ≥ 40 * multigravidas * chronic analgesia use, * allergy to analgesics, * multiple pregnancies are also excluded

Design outcomes

Primary

MeasureTime frameDescription
post operative painone hour after csPost-operative pain is analyzed by using 4 point verbal rating scale (VRS) which consists of a list of adjectives describing different levels of pain intensity i.e (no pain =1, mild pain = 2, moderate pain = 3, severe pain = 4)
intraoperative bleedingfrom skin incision till skin closureThe intra-operative blood loss is evaluated by towels as follows: The surgical towels will be weighed (gm) before and after the operation, and the difference in weight between dry and soaked towels will be calculated. Blood loss during the operation will be calculated by adding the volume of the contents of the suction bottle (ml) to the difference in weight of towels (gm) (weight of soaked towels - weight of dry towels).
The operative time is recorded in minutesfrom skin incision till skin closureThe operative time is recorded in minutes

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026