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Trial · NCT05805683

Calcitonin Therapy on Incidence and Severity of Neuropathic Pain After Spinal Cord Injury

NCT05805683, Not applicable, Recruiting, Tanta University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Calcitonin Therapy on Incidence and Severity of Neuropathic Pain After Spinal Cord Injury. Trials, record NCT05805683. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05805683

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Trial

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

Title
Calcitonin Therapy on Incidence and Severity of Neuropathic Pain After Spinal Cord Injury
NCT number
NCT05805683
Status
Recruiting
Phases
Not applicable
Enrollment
126 participants, estimated
Lead sponsor
Tanta University
Conditions
Calcitonin, Neuropathic Pain, Spinal Cord Injury
Interventions
Calcitonin, Placebo
First posted
2023-04-10
Last updated
2026-05-14

Source ClinicalTrials.gov

Registered outcomes8

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

ListOutcomeTime frameDescription
PrimaryIntensity of neuropathic pain6 months after spinal cord injuryIntensity of neuropathic pain will be evaluated by visual analogue scale (VAS) scores at 6 months after spinal cord injury
PrimaryIncidence of neuropathic pain6 months after spinal cord injuryIncidence of neuropathic pain at 6 months after spinal cord injury
SecondaryIncidence of neuropathic pain12 months after spinal cord injuryIncidence of neuropathic pain at 1, 3, 9 and 12 months after spinal cord injury
SecondaryThe incidence of adverse reactions2 weeks after spinal cord injuryNausea, vomiting, disturbance of serum Calcium, Magnesium and Phosphorus levels
SecondaryThe consumption of medications for neuropathic pain or musculoskeletal pain12 months after spinal cord injuryNumber of patients required medications for neuropathic pain or musculoskeletal pain
SecondaryIntensity of neuropathic pain12 months after spinal cord injuryIntensity of neuropathic pain will be evaluated by the visual analogue scale (VAS) score which ranges from 0 = no pain to 10= worst pain at 12 months after spinal cord injury
SecondaryIntensity of nociceptive pain12 months after spinal cord injuryIntensity of musculoskeletal pain will be evaluated by visual analogue scale (VAS) score which ranges from 0 = no pain to 10= worst pain at 1, 3, 6, 9 and 12 months after spinal cord injury
SecondaryMedications used for neuropathic pain management12 months after spinal cord injuryThe number of medications used for treating neuropathic pain will be recorded

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT05805683

GET https://conductscience.org/api/trials/v1/NCT05805683/registered