Ultrasonography for Nutritional Assesment in Cirrhotic Patients

NCT ID: NCT04099875

Last Updated: 2020-08-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

72 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-04-01

Study Completion Date

2021-04-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Ultrasonography of Rectus Femoris and Anterior Tibialis muscles for nutritional assesment in cirrhotic patients undergoing major abdominal surgery

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

in the study, the investigator will use ultrasound to assess the nutritional state of cirrhotic patients after major abdominal surgery,The investigator aim to assess reliability of ultrasound as a bedside,non invasive tool,The investigator will enroll 72 patients for or study which is an observational study

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Nutrition Assessment

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

ultrasound

Ultrasound is a type of imaging. It uses high-frequency sound waves to look at organs and structures inside the body.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* hepatic patients classified as child A, B undergoing major abdominal surgery (liver resection,whipple,Splenectomy,colectomy, Common Bile Duct exploration,By pass surgery)
* 18-60 yrs old
* no past history of nutritional problems,chronic use of drugs,patients with no orthopedic issues such as skeletal fractures or immobilization

Exclusion Criteria

* Refusal of the patient to share in the study, relevant comorbidities (renal, heart disease or COPD)
* previous immune abnormalities including treatment with corticosteroids
* neuromuscular diseases
* laparoscopic surgery
* patients on parenteral nutrition
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

National Liver Institute, Egypt

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Amany A. Zayd, MBBCH

Role: PRINCIPAL_INVESTIGATOR

Department of Anesthesia NLI

Eman S. Ibrahim, MD

Role: STUDY_DIRECTOR

National Liver Institute

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

National Liver Institute

Shibīn al Kawm, Menoufia, Egypt

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Amany A. Zayd, MBBCH

Role: CONTACT

01014514573

Eman S. Ibrahim, MD

Role: CONTACT

01016303518

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Amany A. Zayd, MBBCH

Role: primary

01014514573

Eman S. Ibrahim, MD

Role: backup

01016303518

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

US in cirrhosis

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.