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Trial Title:
Modulatory Effects of Active Drugs on the Endocannabinoid System on Spontaneous and Induced Contractility of the Colon
NCT ID:
NCT05760404
Condition:
Colorectal Cancer
Conditions: Official terms:
Colorectal Neoplasms
Study type:
Observational
Overall status:
Recruiting
Study design:
Time perspective:
Prospective
Intervention:
Intervention type:
Procedure
Intervention name:
Surgery for colorectal cancer
Description:
Patients undergoing upfront surgery or surgery after neoadjuvant therapy for colorectal
cancer with curative intention
Intervention type:
Other
Intervention name:
in vitro study
Description:
on tissues from colorectal resections
Summary:
The endocannabinoid system plays important roles in the modulation of gastrointestinal
motility and secretions. These effects are mainly mediated by the activation by the
endocannabinoids anandamide (AEA) and 2-arachidonylglycerol (2-AG) of CB1 receptors
expressed on cholinergic neurons. Cannabis sativa extracts also perform these activities,
through the detection of CB1 receptors by the phytocannabinoids they contain, in
particular delta9-tetrahydrocannabinol.
CB1 receptors are abundantly expressed at the synaptic terminals of excitatory motor
neurons and cholinergic secretomotor neurons and their activation induces prejunctional
inhibition of acetylcholine release. It is thought that the endocannabinoids AEA and
2-AG, by activating these receptors, may exert a physiological control on
gastrointestinal contractility and secretions.
This research hypothesizes that drugs capable of inhibiting the biosynthetic and
catabolic enzymes of endocannabinoids, of inhibiting the transmembrane transport of
endocannabinoids or of allosterically modulating CB1 receptors induce important
regulating effects of basal contractility and excitatory motor responses, induced by
activation of neurons intramural cholinergics, of colonic circular smooth muscle.
The effects of drugs acting on CB receptors, endocannabinoid biosynthetic and catabolic
enzymes and endocannabinoid membrane transporters on basal contractility or induced by
neuronal activation of colonic preparations in vitro will be evaluated.
The study will enroll patients affected by colorectal cancer to undergo elective
resective surgery at any stage, undergoing upfront surgery or after neo-adjuvant therapy
with a therapeutic interval greater than 6 weeks. In the selected patients (see
inclusion/exclusion criteria), a fresh sample of about 2.5 cm of healthy colon (healthy
resection margin) will be taken, which will be taken in the operating room and sent to
the laboratory for in vitro study.
Expected results: The study is expected to provide new evidence regarding the induction
of pharmacological effects by allosteric receptor modulators of CB1 receptors, inhibitors
of endocannabinoid biosynthetic and catabolic enzymes, and inhibitors of cannabinoid
transporters in the human colon, which may open interesting perspectives regarding the
development of new therapeutic strategies for the treatment of constipation, diarrhea and
irritable bowel syndrome.
Detailed description:
The present research is aimed at defining the roles of the different components of the
endocannabinoid system in the regulation of the basal contractile activity and of the
excitatory motor responses induced by neuronal activation in the human colon.
Therefore, the motor effects of drugs acting on the various components of this system
will be evaluated, ie receptors, biosynthetic and catabolic enzymes and membrane
transporters, in colonic preparations, in conditions of basal muscle tone and on muscle
contractions induced by neuronal activation.
If the modulation of one or more components of the endocannabinoid system proves to be
important in the regulation of colonic contractility and probably useful for therapeutic
purposes, drugs active on them could represent new treatments for constipation, diarrhea
or some forms of irritable bowel syndrome, very common in the gastrointestinal tract.
Particular interest will be focused on the effects of allosteric modulators of CB1
receptors, inhibitors of biosynthetic and catabolic enzymes of endocannabinoids and
inhibitors of membrane transporters of endocannabinoids.
This is an exploratory study, in which pre-specified hypotheses on pre-specified sample
sizes will not be tested. Therefore, the data will be subjected only to descriptive
statistics, without conducting any tests of statistical significance on them.
Consequently, no primary or secondary endpoints are foreseen.
Criteria for eligibility:
Study pop:
Patients with colorectal cancer at any stage of the disease
Sampling method:
Probability Sample
Criteria:
Inclusion Criteria:
- patients with colorectal cancer at any stage of the disease, undergoing upfront
surgery or neo-adjuvant therapy for more than 6 weeks, to undergo surgery with
resective intent at the UOC of General Surgery 1 of the Fondazione Policlinico
Universitario A. Gemelli of Rome in the two years following the approval of the
study by the Ethics Committee;
Exclusion Criteria:
- patients with diverticular stenosis, patients with stenosing colorectal cancer
(defined as a tumor that cannot be passed through endoscopically, resulting in
clinical and/or radiological symptoms of intestinal obstruction), urgent/emergency
procedures, patients treated with corticosteroid therapy for immuno-rheumatic
diseases, patients treated with radio-chemotherapy and undergone surgery for less
than 6 weeks, surgically resected patients who present macroscopic lesions near the
resection margin when opening the surgical piece, refusal of informed consent.
Gender:
All
Minimum age:
N/A
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
Fondazione Policlinico Universitario A. Gemelli, IRCCS
Address:
City:
Roma
Country:
Italy
Status:
Recruiting
Contact:
Last name:
Roberto Persiani
Start date:
December 19, 2022
Completion date:
December 2024
Lead sponsor:
Agency:
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Agency class:
Other
Source:
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05760404