Trial · NCT02522013
Aminophylline for Patients With Post-Dural Puncture Headache
NCT02522013, Phase 3, Completed, The First Affiliated Hospital of Zhengzhou University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Aminophylline for Patients With Post-Dural Puncture Headache. Trials, record NCT02522013. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02522013
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Aminophylline for Patients With Post-Dural Puncture Headache
- NCT number
- NCT02522013
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 126 participants, actual
- Lead sponsor
- The First Affiliated Hospital of Zhengzhou University
- Conditions
- Post-dural Puncture Headache
- Interventions
- Aminophylline, isotonic saline
- First posted
- 2015-08-13
- Last updated
- 2016-10-31
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | pain on the Visual Analogue Scale | baseline phase | |
| Primary | pain on the Visual Analogue Scale | 0.5 hour after the Intervention | |
| Primary | pain on the Visual Analogue Scale | 1 hour after the Intervention | |
| Primary | pain on the Visual Analogue Scale | 8 hours after the Intervention | |
| Primary | pain on the Visual Analogue Scale | 1 day after the Intervention | |
| Primary | pain on the Visual Analogue Scale | 2 days after the Intervention | |
| Secondary | the overall response to treatment on the Patient Global Impression of Change | 2 days after the Intervention | |
| Other | safety (occurrence of adverse reactions) | Participants will be followed for the duration of hospital stay, an expected average of 7 days | The safety of the IV aminophylline treatment for PDPH was evaluated based on the occurrence of adverse reactions |
Source ClinicalTrials.gov
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.
Papers5
The papers the trial lists on ClinicalTrials.gov.
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.
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/NCT02522013
GET https://conductscience.org/api/trials/v1/NCT02522013/registered