Trial · NCT07877766
Assessing Microbiome in Primary Anterior Cervical Fusion Patients
NCT07877766, Not applicable, Enrolling by invitation, Hospital for Special Surgery, New York
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Assessing Microbiome in Primary Anterior Cervical Fusion Patients. Trials, record NCT07877766. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07877766
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Assessing Microbiome in Primary Anterior Cervical Fusion Patients
- NCT number
- NCT07877766
- Status
- Enrolling by invitation
- Phases
- Not applicable
- Enrollment
- 76 participants, estimated
- Lead sponsor
- Hospital for Special Surgery, New York
- Conditions
- Cervical Stenosis, Myelopathy, Cervical Spondylosis With Myelopathy, Degenerative Disc Disease, Radiculopathy
- Interventions
- Primary Anterior Cervical Discectomy Procedures
- First posted
- 2026-10-16
- Last updated
- 2026-10-16
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Metagenomic sequencing to assess bacterial presence | perioperative | Metagenomic sequencing will be compared to microbiological cultures |
| Secondary | Visual Analog Scale (VAS) for Neck and Arm Pain | Up to 1 year postoperatively | Neck pain and arm pain (left and right arms rated separately) will be assessed using a 100 mm Visual Analog Scale (VAS). Scores range from 0 mm (no pain) to 100 mm (worst possible pain). Higher scores indicate more severe pain (a worse outcome). |
| Secondary | Neck Disability Index (NDI) Score | Up to 1 year postoperatively | The Neck Disability Index (NDI) is a 10-item questionnaire that measures how neck pain affects daily activities. Each item is scored from 0 to 5, and the total score (0 to 50) is expressed as a percentage ranging from 0% (no disability) to 100% (complete disability). Higher scores indicate greater disability (a worse outcome). |
| Secondary | Number of Participants With Radiographic Fusion | Up to 1 year postoperatively | Fusion status at the operative level(s) will be assessed using standard-of-care postoperative plain radiographs (X-ray) and computed tomography (CT) scans. |
| Secondary | Number of Participants With Radiographic Evidence of Screw Lucency or Loosening | Up to 1 year postoperatively | Radiographic evidence of lucency (radiolucency) around screws or implant loosening at the operative level(s) will be assessed using standard-of-care postoperative plain radiographs (X-ray) and computed tomography (CT) scans. |
| Secondary | Adverse events | Up to 1 year postoperatively | To categorize any surgery-related adverse events |
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.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 32453165 | BACKGROUND |
Source PubMed
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/NCT07877766
GET https://conductscience.org/api/trials/v1/NCT07877766/registered