A Modified Approach for the Closure of Oral Sinus Communications

See also
Status	Clinical Trial	Phase
Recruiting	`NCT05350540` - Hypopharynx ICG to Reduce the Fistula Rate in Patients Undergoing Salvage Laryngectomy	Phase 2
Recruiting	`NCT04136522` - Usefulness of the Artery First Approach in Pancreatic Cancer Surgery	N/A
Completed	`NCT04771832` - ERAS in Gastrointerstinal Fistulas.
Completed	`NCT03410914` - Intra-operative Application of HEMOPATCH to the Pancreatic Stump to Prevent Post-operative Pancreatic Fistula Following Distal Pancreatectomy	Phase 2

See also

Status

Clinical Trial

Phase

Recruiting

NCT05350540 - Hypopharynx ICG to Reduce the Fistula Rate in Patients Undergoing Salvage Laryngectomy

Phase 2

Recruiting

NCT04136522 - Usefulness of the Artery First Approach in Pancreatic Cancer Surgery

N/A

Completed

NCT04771832 - ERAS in Gastrointerstinal Fistulas.

Completed

NCT03410914 - Intra-operative Application of HEMOPATCH to the Pancreatic Stump to Prevent Post-operative Pancreatic Fistula Following Distal Pancreatectomy

Phase 2

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT04499144
Study type	Interventional
Source	University of Siena
Contact
Status	Completed
Phase	N/A
Start date	June 26, 2020
Completion date	July 27, 2020

A Modified Approach for the Closure of Oral Sinus Communications

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms