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Liver Transplant; ComplicationsLDLTNCT06542913

Left Lobe Versus Right Lobe in Adult Living Donor Liver Transplantation in Borderline GRWR

An observational study of Liver Transplant; Complications, run by Ain Shams University.

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 The sponsor has not verified this record for over two years, so it may be out of date.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

a prospective cohort study comparing outcomes of left lobe and right lobe adult living donor liver transplantation Read more about this study

Who is it for?
Ages 16 to 65 years
Conditions the study is for
Liver Transplant; Complications
How many people
30 participants
Where
No sites listed yet
Study dates
15 Sep 2024to 15 Jun 2026
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 16 to 65 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: patients presented to our center for LDLT

Who may be able to join

  • GRWR below 1

Who cannot join

  • patients with renal impairment portal vein thrombosis vascular complications

Trial locations and contacts

No sites are listed yet.

Ibrahim Essam, M.Sc. MRCS contact

00201001805340

ibrahim.essam@med.asu.edu.eg

About this study

Official title: Left Lobe Versus Right Lobe in Adult Living Donor Liver Transplantation in Borderline GRWR: Prospective Cohort Study

a prospective cohort study comparing outcomes of left lobe and right lobe adult living donor liver transplantation

What participants receive

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

Study groups in NCT06542913
Study groupRoleWhat they receive
right lobecases underwent LDLT for right lobe with borderline GRWR
left lobecases underwent LDLT for left lobe with borderline GRWR

What is being measured

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

  1. small for size syndrome

    small for size syndrome

    Measured: 1 year

Secondary outcomes (1)
  1. other complications after LDLT

    other complications after LDLT

    Measured: 1 year

Timeline

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

  1. First posted7 Aug 2024
  2. Study start15 Sep 2024 (estimated)
  3. Primary completion15 Jun 2026 (estimated)
  4. Study completion15 Jun 2026 (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
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06542913
Sponsor's protocol ID
ltvsrtldlt
Other IDs
Ain Shams University
Acronym
LDLT
Status last verified
Aug 2024
First submitted
3 Aug 2024
Last updated
7 Aug 2024
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Liver Transplant; Complications, run by Ain Shams University.

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 7 Aug 2024. Status can change between updates, so confirm with the study contact before making plans.

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?

Contact Ibrahim Essam, M.Sc. MRCS (00201001805340, ibrahim.essam@med.asu.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

small for size syndrome (time frame: 1 year). 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 7 Aug 2024.

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