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Trial · NCT03918187

Intrathecal Nalbuphine Versus Midazolam in Cesarean Section

NCT03918187, Phase 1, Completed, Zagazig University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Intrathecal Nalbuphine Versus Midazolam in Cesarean Section. Trials, record NCT03918187. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03918187

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Intrathecal Nalbuphine Versus Midazolam in Cesarean Section
NCT number
NCT03918187
Status
Completed
Phases
Phase 1
Enrollment
90 participants, actual
Lead sponsor
Zagazig University
Conditions
Cesarean Section Pain
Interventions
Bupivacaine, Nalbuphine, Midazolam
First posted
2019-04-17
Last updated
2019-12-24

Source ClinicalTrials.gov

Registered outcomes7

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryEffective analgesic timeup to six hours postoperativethe time start from intrathecal injection to the first analgesic dose.
PrimaryTotal postoperative analgesic dose .24 hoursthe analgesic dose consumed
PrimaryOnset of sensory and motor blockup tp five minutes after intrathecal injectionthe time of onset of sensory and motor block
Primaryduration of sensory and motor blockup to five hours postoperativethe time of duration of sensory and motor block
SecondarySedation scoreone hour during surgery
score of sedation: 1= awake and alert 2 = sedated ,respond to verbal stimules 3= sedated respond to a mild physical status 4=sedated respond to a moderate or strong physical stimuls 5= not arousable 5 is the higher value
SecondaryApgar score1-5 minutes after deliveryscore for baby
Secondarynumber of participants with hypotension , bradycardia ,vomiting , nausea , shivering number of participants with hypotension , bradycardia ,vomiting , nausea , shiveringup to 24 hours postoperativeincidence of hypotension , bradycardia ,vomiting , nausea , shivering

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
32606903DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT03918187

GET https://conductscience.org/api/trials/v1/NCT03918187/registered