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Prospective interventional study to assess the impact of introducing an Enhanced Recovery After Surgery (ERAS) program on post-operative complications and prognosis in patients with oral surgical diseases

Prospective interventional study to assess the impact of introducing an Enhanced Recovery After Surgery (ERAS) program on post-operative complications and prognosis in patients with oral surgical diseases - Kagoshima University Oral Surgery ERAS Protocol

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000056803
Enrollment
800
Registered
2025-02-01
Start date
2025-02-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients undergoing surgery under general anaesthesia at the Department of Oral Surgery, Kagoshima University Hospital

Interventions

Preoperative drinking of oral rehydration fluid (clarified water with whey protein or clarified water with maldextrin)

Sponsors

Kagoshima University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients undergoing surgery under general anaesthesia for diseases of the oral and maxillofacial region

Exclusion criteria

Exclusion criteria: (i) Cases with active infections (tuberculosis, viral or fungal infections). (ii) Cases with a history of poorly controlled diabetes mellitus such as type 1 diabetes mellitus (iii) Patients taking steroids due to autoimmune diseases (iv) Cases with allergy to steroids (v) Women who are pregnant, possibly pregnant, within 28 days postpartum or breastfeeding (vi) Cases with thrombosis, poorly controlled glaucoma or active gastrointestinal ulcer (vii) Subjects deemed unlikely to participate in the study due to psychosis or psychiatric symptoms (viii) Other subjects deemed ineligible by the doctor/dentist.

Design outcomes

Primary

MeasureTime frame
(i) Post-operative hospital stay (number of days until the patient is diagnosed as ready for discharge). (ii) Postoperative complications (pain, bleeding, postoperative infection, wound healing, postoperative nausea and vomiting, organ damage, degree of invasion) (iii) Prognosis (overall survival, disease-specific survival, disease-free survival).

Secondary

MeasureTime frame
(i) timing and method of initiation of oral and enteral nutrition (including level of independence in nutritional intake) 2) Patient satisfaction (assessment of quality of life) (iii) ERAS achievement rate (iv) Level of independence at discharge (5) Volume of infusion (In/Out balance) (vi) Inflammatory reaction due to surgery

Countries

Japan

Contacts

Public ContactRyota Takaoka

Kagoshima University Oral surgery

179618132ryota@gmail.com099-275-6232

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026