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Urinary TitinNCT06487728

The Validity of Urinary Titin and Skeletal Muscle Index as Predictor of Muscle Weakness in Critically Ill Patients. A Prospective Cohort Study

An observational study of Urinary Titin, run by Zagazig University at 1 site in Egypt.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Although skeletal muscle atrophy is common in critically ill patients, biomarkers associated with muscle atrophy have not been identified reliably. Titin is a spring-like protein found in muscles and has become a measurable biomarker for muscle breakdown and intensive care unit-acquired weakness in critically ill… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Urinary Titin
What is being tested?
Urinary titin
How many people
161 participants
Where
1 siteEgypt
Study dates
1 Jul 2024to 1 Feb 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Critically ill patients

Who may be able to join

  • Consent from relatives of first degree. Consecutive adult patients who will be expected to remain in ICU for >5 days will be enrolled. Nonsurgical critically ill patients will be included because surgical insult reportedly increased urinary titin level (Tanihata et al., 2019). Age more than 18 years. Both male and female.

Who cannot join

  • Surgery not including percutaneous abscess drainage. Patients with expected prehospital functional status of <48 hours. Chest tube insertion, and tracheostomy in ICU. 8 Current pregnancy. Diagnosis of primary neuromuscular disease. Trauma at the measurement point.

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Faculty of medicine, Zagazig university

    Zagazig, Sharqia Province

Other trials in Egypt

About this study

Although skeletal muscle atrophy is common in critically ill patients, biomarkers associated with muscle atrophy have not been identified reliably. Titin is a spring-like protein found in muscles and has become a measurable biomarker for muscle breakdown and intensive care unit-acquired weakness in critically ill patients, in whom titin loss is a possible pathophysiology. The skeletal muscle index (SMI) is an alternative biomarker for muscle weakness, which is calculated by dividing the cross-sectional area (cm2) of the skeletal muscle at the level of the third lumbar vertebra by the square of the patient's height (m2) on CT The possibility of using urinary titin and skeletal muscle index for early prediction of muscle weakness in critically ill patients.

Read the detailed description

All patients will be subjected to the following:

Informed consent will be obtained from patients. History taking including age, sex, comorbidities, current medications, ethnicity, reason for admission, and body mass index (BMI). General clinical examination. General laboratory investigations: (CBC, Random blood sugar, CRP, ESR).

Urinary Titin Measurement:

The first urine sample will be collected using a urethral catheter within 12 h of ICU admission and 24-hour urine samples d 24-hour urine samples on days 2, 3, 5, and 7.

Urinary titin will be measured using an ELISA kit (Maruyama et al., 2016).

Skeletal Muscle Index calculation:

This assessment calculates the skeletal muscle index (SMI) (cm2/m2) by dividing the cross-sectional area (cm2) of the skeletal muscle at the level of the third lumbar vertebra (L3) by the square of the patient's height (m2) on CT. SMI measured using CT. ( Mitobe et al. 2019).

Ultrasonographic Measurement:

Rectus femoris muscle area and diaphragm thickness will be evaluated with serial ultrasound measurements on days 1, 3, 5, and 7 of ICU admission. Recordings will be discontinued at death or ICU discharge. Cross-sectional area of the rectus femoris muscle will be evaluated at the midway between the anterior superior iliac spine and the proximal 9 end of the patella. A transducer will be placed perpendicularly to the long axis of the rectus femoris muscle with patients in the supine position under passive knee extension.

The diaphragm will be evaluated at the zone of apposition on the right chest wall. Its thickness will be measured during the end-expiration phase. Beds will be adjusted at a 30° angle. We will exclude patients whose diaphragm is unclear or difficult to measure.

Patients will be divided into three groups according to the changes in diaphragm thickness: atrophy, unchanged, and increased. A 10% change in diaphragm thickness will be regarded as the cutoff value in the three groups. Atrophy will be first classified with >10% decrease in diaphragm thickness from day 1 to the lowest value over the measurement period. Thereafter, increased thickness group will be classified when >10% increase is observed. The rest of the patients were classified into the unchanged group, as previously reported (Nakanishi et al., 2019). In the analysis, the unchanged group will be compared with atrophy and increased groups and their combination because both increased and decreased diaphragm thickness significantly influence clinical outcomes (Goligher et al., 2018). Rectus femoris cross-sectional area and diaphragm thickness will be measured thrice, and the median value was used for evaluation. All measurements will be conducted by two examiners. Intraclass and interclass correlation coefficients will be 0.99 and 0.99 for rectus femoris cross-sectional area and 0.95 and 0.95 for diaphragm thickness, respectively.

Physical Assessment and Mobilization:

When patients are awake and attentive, physical therapists will be evaluated the Medical Research Council (MRC) score and incidence of ICU-AW on days 1 and 7 of ICU admission. Intact level of consciousness and awareness will be defined by patient's response to at least three of five orders (De Jonghe et al., 2007).

ICU-AW will be defined as an MRC score of <48 on two separate occasions (Stevens et al., 2009). We will use the incidence of ICU-AW following the last measurement for comparison. 10 IMS is a measure of mobilization capabilities from 0 (lying in bed) to 10 (walking independently) (Hodgson et al., 2014). We will evaluate maximum IMS score during the study period because the maximum level of mobility is an important prognostic factor (Kim et al., 2019).

Conditions
Urinary Titin
Being tested
Urinary titin

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Urinary titinDiagnostic test

    Urinary titin and skeletal muscle index as predictor of muscle wasting in critically ill patient

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The relationship between cumulative urinary titin level and rate of rectus femoris muscle atrophy on days 1 and 7 of ICU admission

    Measurement of urinary titin level and its correlation to muscle index

    Measured: At day 1 and 7 day of icu admission

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Jul 2024
  2. Study start1 Jul 2024 (estimated)
  3. Primary completion1 Jan 2025 (estimated)
  4. Study completion1 Feb 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
161 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06487728
Sponsor's protocol ID
386/10-June 2024
Status last verified
Jun 2024
First submitted
27 Jun 2024
Last updated
5 Jul 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Urinary Titin, run by Zagazig University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 5 Jul 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The relationship between cumulative urinary titin level and rate of rectus femoris muscle atrophy on days 1 and 7 of ICU admission (time frame: At day 1 and 7 day of icu admission). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Jul 2024; AzTrials last refreshed its copy on 8 Nov 2026.

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