Epidural Hydroxyethyl Starch for Post-Dural Puncture Headache in Parturients
NCT07914790, Recruiting, Peking University First Hospital
Trial 9
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Epidural Hydroxyethyl Starch for Post-Dural Puncture Headache in Parturients | ClinicalTrials.gov |
| NCT number | NCT07914790 | ClinicalTrials.gov |
| Status | Recruiting | ClinicalTrials.gov |
| Enrollment | 410 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Peking University First Hospital | ClinicalTrials.gov |
| Conditions | Parturients, Accidental Puncture of Dura During Anaesthesia, Epidural Filling, Hydroxyethyl Starch, Post-dural Puncture Headache | ClinicalTrials.gov |
| Interventions | Epidural hydroxyethyl starch, No epidural hydroxyethyl starch | ClinicalTrials.gov |
| First posted | 2026-11-04 | ClinicalTrials.gov |
| Last updated | 2026-11-06 | ClinicalTrials.gov |
Registered outcomes 3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Incidence of post-dural puncture headache (PDPH) within 7 days. | Up to 7 days after accidental dural puncture. | According to the International Classification of Headache Disorders, 3rd edition (ICHD-3) diagnostic criteria for post-dural puncture headache (PDPH), PDPH is defined as: a history of dural puncture; headache occurring within 5 days after dural puncture; headache consistent with low cerebrospinal fluid pressure headache; and not better accounted for by another ICHD-3 diagnosis. | ClinicalTrials.gov |
| Secondary | Duration of post-dural puncture headache (PDPH) | Up to 2 weeks after accidental dural puncture. | Duration of PDPH is defined as the time from the onset of PDPH to complete resolution of headache, recorded in days. Patients without resolution by the end of follow-up will be censored at the last follow-up visit. | ClinicalTrials.gov |
| Secondary | Severity of post-dural puncture headache (PDPH) | Up to 2 weeks after accidental dural puncture. | PDPH severity was graded on a 0-10 numeric rating scale (NRS) as mild (1-3), moderate (4-6), or severe (7-10). | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 26
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|---|---|
| 7517925 | BACKGROUND | PubMed |
| 9349072 | BACKGROUND | PubMed |
| 9512843 | BACKGROUND | PubMed |
| 15321604 | BACKGROUND | PubMed |
| 16738294 | BACKGROUND | PubMed |
| 18691871 | BACKGROUND | PubMed |
| 23474278 | BACKGROUND | PubMed |
| 25907209 | BACKGROUND | PubMed |
| 26221406 | BACKGROUND | PubMed |
| 26950232 | BACKGROUND | PubMed |
| 27378709 | BACKGROUND | PubMed |
| 28131118 | BACKGROUND | PubMed |
| 29368949 | BACKGROUND | PubMed |
| 29420792 | BACKGROUND | PubMed |
| 29492450 | BACKGROUND | PubMed |
| 31335402 | BACKGROUND | PubMed |
| 31524925 | BACKGROUND | PubMed |
| 32858584 | BACKGROUND | PubMed |
| 33021807 | BACKGROUND | PubMed |
| 33725362 | BACKGROUND | PubMed |
Grants 0
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)