Research

We have an internationally recognised research unit
based at the University of Liverpool

The Liverpool Clinical Trials Centre's portfolio of studies is displayed below.

As part of each study, the LCTC collects information about study participants and research team members – please click here to access the LCTC Privacy Notice which provides more information on how we use Personal Data.

LCTC supports sharing of anonymised data for secondary research. For the studies displayed below which are completed researchers may submit initial queries to lctc@liverpool.ac.uk. Further details on Data Sharing activities by LCTC can be found here on our website.

Logo
ACELARATE

A Phase III, open label, multicentre randomised clinical study comparing Acelarin (NUC-1031) with Gemcitabine in patients with metastatic pancreatic carcinoma.

Logo
ACIT-1

A Phase I clinical study to determine the optimal dose for the safe immune restoration and immune response of allogeneic cell immunotherapy (ACIT-1) in adult cancer patients.

Logo
APPA

A Phase I, Partially Blind, Placebo-Controlled, Ascending Single and Multiple Oral Dose, Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study in Healthy Subjects and Osteoarthritis Patients administered APPA-1

Logo
APRiCOT

A Pilot Randomised Study to Compare Combination Antibiotic Therapy (Ciprofloxacin, Doxycycline and Hydroxychlororquine) with Standard Therapy (Budesonide) in the Treatment of Active Crohn's Disease

Logo
APTITUDE

A phase II trial of Tocilizumab in anti-TNF refractory patients with JIA associated uveitis

Logo
ATTAINMENT

A modular, multi-arm, first in human trial to evaluate the safety and tolerability of MDX-124 alone and in combination with anti-cancer treatments, in participants with locally advanced, unresectable or metastatic solid malignancies

Logo
BASICS

Antibiotic and Silver Impregnated Catheters for ventriculoperitoneal Shunts (BASICS): a multi-centre randomised controlled trial

Logo
BESS

the use of surfactant for babies with severe bronchiolitis on PICU

Logo
BIOPROP20

Biologically optimised IMRT for Prostate Radiotherapy Hypofractionated radiotherapy with intra-prostatic boosts to tumour nodules in men with intermediate and high risk prostate cancer

Logo
BOSS

Investigating Slipped Capital Femoral Epiphysis (SCFE) as a childhood precursor to osteoarthritis of the hip in adulthood: A nationwide service evaluation, and nested-cohort study

Logo
CAPER

A Phase Ib clinical trial of Cyclophosphamide And PEmbrolizumab in metastatic Renal cell carcinoma (CAPER Trial)

Logo
CASTLE

Randomised factorial design controlled trial comparing carbamazepine, levetiracetam or active monitoring combined with or withou

Filter by Portfolio:
  • 42
  • 37
  • 3
  • 30
  • 14
Filter by intervention:
  • 6
  • 70
  • 36
  • 9
Writing a Statistical Analysis Plan
As well as managing studies we regularly work with methodologists to undertake research aimed at improving the design and delivery of clinical trials. One such project is the Statistical Analysis Plan (SAP) Guidelines.

Increasing calls for transparency, reproducibility and data sharing within clinical trials have led to a greater emphasis on the early development and publication of well written Statistical Analysis Plans (SAPs).

To address a variation in practice a minimum set of items for SAPs was agreed with funders, regulatory authorities, journals and researchers. A downloadable version of the SAP checklist is available here.

Collaborate with us
We specialise in the development and delivery of large, multi-centre clinical trials.