Trial · NCT07906210
Therapeutic Holding Versus Traditional Restraint During Pediatric Venipuncture
NCT07906210, Not applicable, Not yet recruiting, University of Baghdad
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Therapeutic Holding Versus Traditional Restraint During Pediatric Venipuncture. Trials, record NCT07906210. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07906210
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Therapeutic Holding Versus Traditional Restraint During Pediatric Venipuncture
- NCT number
- NCT07906210
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 64 participants, estimated
- Lead sponsor
- University of Baghdad
- Conditions
- Pediatric Venipuncture
- Interventions
- Therapeutic Holding, Traditional Restraint
- First posted
- 2026-10-30
- Last updated
- 2026-10-30
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Behavioral Distress Across Venipuncture Phases Measured by the PBRS-R | Before positioning and before needle insertion; at needle insertion; and after needle removal and completion of venipuncture. | Children's behavioral distress will be assessed using the Procedure Behavior Rating Scale-Revised (PBRS-R). Eleven observable distress behaviors are recorded as present or absent across three procedural phases. The total PBRS-R score ranges from 0 to 33, with higher scores indicating greater behavioral distress. |
| Primary | Pulse Rate Across Venipuncture Phases | Before application of the assigned holding/restraint method; during venipuncture; and after completion of venipuncture. | Pulse rate, measured in beats per minute using a pulse oximeter, will be recorded to assess physiological response and stability across the procedural phases. |
| Primary | Respiratory Rate Across Venipuncture Phases | Before application of the assigned holding/restraint method; during venipuncture; and after completion of venipuncture. | Respiratory rate, measured in breaths per minute by direct observation, will be recorded to assess physiological response and stability across the procedural phases. |
| Primary | Oxygen Saturation (SpO₂) Across Venipuncture Phases | Before application of the assigned holding/restraint method; during venipuncture; and after completion of venipuncture. | Peripheral oxygen saturation (SpO₂), expressed as a percentage and measured using a pulse oximeter, will be recorded to assess physiological response and stability across the procedural phases. |
| Primary | First-Stick Venipuncture Success | During the venipuncture procedure. | First-stick venipuncture success is defined as obtaining the required blood sample following the first needle penetration of the skin. The number of attempts will also be recorded. Each new needle penetration through the skin will be considered a new attempt, whereas redirection of the needle while it remains beneath the skin will not be considered an additional attempt. |
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.
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.
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/NCT07906210
GET https://conductscience.org/api/trials/v1/NCT07906210/registered