Early Feeding TL Trial
NCT07919821, Phase 2, Not yet recruiting, University of Florida
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Early Feeding TL Trial | ClinicalTrials.gov |
| NCT number | NCT07919821 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Phases | Phase 2 | ClinicalTrials.gov |
| Enrollment | 120 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | University of Florida | ClinicalTrials.gov |
| Conditions | Total Laryngectomy | ClinicalTrials.gov |
| Interventions | oral intake | ClinicalTrials.gov |
| First posted | 2026-11-05 | ClinicalTrials.gov |
| Last updated | 2026-11-05 | ClinicalTrials.gov |
Registered outcomes 10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Early oral feeding versus delayed oral feeding. | post-operative days 14 (± 7 days) and 30 (± 7 days). | Comparison of dysphagia-related outcomes in patients who have received early versus delayed oral feeding pre-operatively (if available) | ClinicalTrials.gov |
| Primary | MD Anderson Dysphagia Inventory (MDADI) total score | post-operative days 14 (± 7 days) and 30 (± 7 days). | Questionnaire: Assess dysphagia's effects on the quality of life (QOL) of patients with head and neck cancer. | ClinicalTrials.gov |
| Primary | Summary measure | post-operative days 14 (± 7 days) and 30 (± 7 days). | Difference in mean MDADI scores between groups over time, | ClinicalTrials.gov |
| Secondary | Pharyngocutaneous fistulas | within 30 days of surgery | Proportion of patients who develop postoperative complications requiring invasive intervention (surgical or bedside) . salivary leak, | ClinicalTrials.gov |
| Secondary | Surgical site infections | within 30 days of surgery | Proportion of patients who develop postoperative complications requiring invasive intervention (surgical or bedside) . | ClinicalTrials.gov |
| Secondary | Wound dehiscence | within 30 days of surgery | Postoperative complications proportion of patients who develop postoperative complications requiring invasive intervention (surgical or bedside) . | ClinicalTrials.gov |
| Secondary | Length of stay | within 30 days of surgery | Hospital-based metrics documented in the electronic medical record. | ClinicalTrials.gov |
| Secondary | Enteral feeding duration | within 30 days of surgery | Hospital-based metrics documented in the electronic medical record. | ClinicalTrials.gov |
| Secondary | Rate of oral tolerance | within 30 days of surgery | Hospital-based metrics documented in the electronic medical record. | ClinicalTrials.gov |
| Secondary | Performance Status Scale for Head and Neck Cancer | within 30 days of surgery | Clinician-rated assessment tool. Each subscale is scored from 0 to 100, where 100 represents the best possible performance or normalcy of function, and lower scores reflect greater impairment. | 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 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
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)