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Trial · NCT07912866

Efficacy Of Supplemental L-Arginine in Preventing Preeclampsia in Pregnant Women

NCT07912866, Not applicable, Completed, Quaid-e-Azam Medical College

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Efficacy Of Supplemental L-Arginine in Preventing Preeclampsia in Pregnant Women. Trials, record NCT07912866. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07912866

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Trial

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

Title
Efficacy Of Supplemental L-Arginine in Preventing Preeclampsia in Pregnant Women
NCT number
NCT07912866
Status
Completed
Phases
Not applicable
Enrollment
108 participants, actual
Lead sponsor
Quaid-e-Azam Medical College
Conditions
Pre-eclampsia
Interventions
L-Arginine, placebo
First posted
2026-11-03
Last updated
2026-11-03

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryPercentage of Participants Who Remained Free of Preeclampsia Until DeliveryFrom enrollment at 20 weeks of gestation until delivery,
Efficacy was measured as the percentage of participants in each study group who did not develop preeclampsia before delivery. According to the synopsis, preeclampsia was defined as new-onset systolic blood pressure \>140 mmHg and diastolic blood pressure \>90 mmHg, together with urinary protein excretion \>300 mg over 24 hours, after 20 weeks of gestation in previously normotensive women.

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.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

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.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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/NCT07912866

GET https://conductscience.org/api/trials/v1/NCT07912866/registered