Trial · NCT04343170
Effect of Ultra-short-term Treatment of Patients With Iron Deficiency or Anemia Undergoing Adolescent Scoliosis Correction
NCT04343170, Not applicable, Completed, Tanta University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effect of Ultra-short-term Treatment of Patients With Iron Deficiency or Anemia Undergoing Adolescent Scoliosis Correction. Trials, record NCT04343170. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04343170
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effect of Ultra-short-term Treatment of Patients With Iron Deficiency or Anemia Undergoing Adolescent Scoliosis Correction
- NCT number
- NCT04343170
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 44 participants, actual
- Lead sponsor
- Tanta University
- Conditions
- Ultra-short-term, Iron Deficiency Anemia, Scoliosis Idiopathic
- Interventions
- Placebo, ferric carboxymaltose , α erythropoietin, vitamin B12, oral folic acid
- First posted
- 2020-04-13
- Last updated
- 2025-04-16
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | percentage of patients not required blood transfusion | up to 7 days postoperative | percentage of patients not required blood transfusion |
| Secondary | the length in I.C.U | during ICU stay period up to 7 days postoperative | the length in I.C.U by days |
| Secondary | the incidence of acute kidney injury | up to 7 days postoperative | number of patients developed acute kidney injury |
| Secondary | incidence of infections requiring antibiotic treatment | up to 7 days postoperative | number of patients developed infections requiring antibiotic treatment |
| Secondary | perioperative hemoglobin | up to 7 days postoperative | perioperative hemoglobin by gm |
| Secondary | perioperative platelet | up to 7 days postoperative | perioperative platelet presented as platelet count per microliter of blood |
| Secondary | perioperative leucocyte counts | up to 7 days postoperative | perioperative leucocyte counts presented as white blood cells per microliter |
| Secondary | calculated Red blood cells loss | up to 7 days postoperative | calculated Red blood cells loss by ml |
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/NCT04343170
GET https://conductscience.org/api/trials/v1/NCT04343170/registered