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NCT Number: NCT07545694

Study on the Effects of Drugs That Modulate the Endocannabinoid System on Spontaneous and Induced Contractility of the Human Detrusor Muscle

The goal of this observational, in vitro study is to evaluate the effects of drugs that modulate the endocannabinoid system on spontaneous and neuronally induced contractility of the human detrusor. The study will include adult patients undergoing elective radical cystectomy for bladder cancer. The main questions it aims to answer are whether modulation of endocannabinoid receptors, enzymes involved in endocannabinoid synthesis and degradation, and endocannabinoid transport mechanisms alters basal detrusor contractility and modifies excitatory motor responses induced by neuronal activation.

Participants undergoing radical cystectomy will provide written informed consent for the collection of a small sample of macroscopically healthy bladder tissue from the surgical specimen. Detrusor muscle strips will be prepared and studied in vitro using organ bath techniques. Contractile activity will be recorded under baseline conditions and after electrical field stimulation, as well as following exposure to pharmacological modulators of the endocannabinoid system. Demographic, clinical, and pathological data will also be collected for descriptive analysis.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Largo A. Gemelli, 100168 - Roma

Rome, Italy

Location status: Recruiting

Location contact

Maria Chiara Sighinolfi, Dr.

CONTACT

About this study

This is a prospective, monocentric, observational in vitro study designed to investigate the role of the endocannabinoid system in the regulation of human detrusor contractility. The study evaluates the effects of pharmacological modulation of endocannabinoid receptors, enzymes involved in endocannabinoid synthesis and degradation, and endocannabinoid transport mechanisms on both spontaneous and neuronally induced contractile activity of human detrusor muscle.

The endocannabinoid system has been implicated in the regulation of lower urinary tract function, including sensory signaling and smooth muscle contractility. Experimental evidence suggests that cannabinoid receptor activation may modulate neurotransmitter release and detrusor muscle activity. However, most available data derive from animal models, and findings in human tissues remain limited and sometimes conflicting. A better characterization of the role of endocannabinoid signaling in human detrusor contractility may provide insight into potential therapeutic targets for disorders such as detrusor overactivity and overactive bladder syndrome.

Bladder tissue samples will be obtained from surgical specimens and processed for in vitro functional studies. Detrusor muscle strips will be prepared and mounted in organ baths to record contractile responses under controlled experimental conditions. Baseline motor activity and responses to neuronal stimulation will be assessed. Preparations will then be exposed to pharmacological agents acting on different components of the endocannabinoid system, including receptor agonists and antagonists, allosteric modulators, inhibitors of endocannabinoid biosynthesis and degradation, and inhibitors of endocannabinoid transport. Changes in contractile activity will be evaluated to characterize the functional contribution of these pathways.

The experimental procedures will be conducted in sequential phases to characterize baseline contractile responses, assess receptor-mediated effects, and evaluate the impact of modulation of endocannabinoid metabolism and transport. Clinical and demographic data will be recorded for descriptive purposes. The study is exploratory in nature and aims to generate mechanistic data on the role of the endocannabinoid system in human detrusor physiology.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years.
  • Patients with bladder carcinoma at any stage of disease, undergoing upfront surgery or neoadjuvant therapy for more than 6 weeks, scheduled for surgery with curative/demolitive intent.
  • Signed written informed consent to participate in the study.

Exclusion criteria

  • Age < 18 years.
  • Procedures performed on an urgent/emergency basis.
  • Patients treated with corticosteroid therapy for immunorheumatic diseases.
  • Patients treated with radio-chemotherapy and undergoing surgery less than 6 weeks prior.
  • Refusal to sign written informed consent to participate in the study.

Treatment and study plan

Primary outcomes

  1. Effects of CB receptor agonists, antagonists and allosteric modulators, endocannabinoid synthesis/catabolism enzyme inhibitors, and EMT transporter inhibitors on EFS-induced submaximal contractions of detrusor preparations

    Time frame: Time of in vitro organ bath pharmacological assessment (during the 30-month study period, post-tissue collection)

    Evaluate the change in amplitude on submaximal contractions induced by electrical field stimulation (EFS) in human detrusor tissue strips mounted in organ baths following exposure to specified drugs

Study contacts

Contact information is provided by the study sponsor or research team.

MARIA CHIARA SIGHINOLFI, DR

CONTACT

[email protected]

0039 3921329216

Sponsors and collaborators

Lead sponsor

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Other

Registry information

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
Apr 22, 2026
Registry last updated
Apr 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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