Actively Recruiting

Age: 18Years +
All Genders
NCT07125859

Malnutrition Prevalence and Nutritional Change After Preoperative Nutrition Counseling

Led by Siriraj Hospital · Updated on 2026-02-27

600

Participants Needed

1

Research Sites

50 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Preoperative nutrition risk or Malnutrition is a prevalent up to 65% of surgical patients, leading to significant negative outcomes such as increased complications, poor wound healing, and higher healthcare costs. Preoperative nutrition status is a modifiable risk factor that can be optimized to improve surgical outcomes. Preoperative malnutrition screening creates an opportunity to identify and optimize the nutritional status of at-risk patients before surgery. This study is initiated to determine the prevalence of malnutrition among surgical patients enrolled in an Enhanced recovery after surgery (ERAS) program, using the SPENT and modified Nutrition Alert Form (NAF) during their visit to the preoperative clinic and evaluate the impact of preoperative nutrition education on body weight and nutrition status prior to surgery.

CONDITIONS

Official Title

Malnutrition Prevalence and Nutritional Change After Preoperative Nutrition Counseling

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 618 years.
  • Enrolled in the Enhanced Recovery After Surgery (ERAS) program.
  • Referred to the SiPAP program for prehabilitation before elective surgery.
  • Screened for malnutrition risk using the Society of Parenteral and Enteral Nutrition of Thailand (SPENT) screening tool.
  • Complete clinical records available for analysis.
Not Eligible

You will not qualify if you...

  • Incomplete nutritional records.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Faculty of Medicine Siriraj Hospital

Bangkok, Thailand, 10700

Actively Recruiting

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Research Team

M

Mingkwan Wongyingsinn, MD

CONTACT

P

Parujee Nakjuy, BSc

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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