Obesity, AbdominalOBESENCT05966727
Exploratory Evaluation of the Effect of Cholestyramine on Serum Levels of POPs in Obese Female Patients
A study testing Cholestyramine Powder in people with Obesity, Abdominal and Diabetes, run by Centre Hospitalier Universitaire de Nice at 1 site in France.
Trial summary
Environmental endocrine disruptors (EDCs) represent a major problem for human health.Some PEEs can accumulate in the fatty tissue of the human body thanks to their lipophilic nature, and are known as persistent organic pollutants (POPs). Read more about this study
- Who is it for?
- Ages 18 to 45 years, women only
- Conditions the study is for
- Obesity, Abdominal, Diabetes, Bariatric Surgery Candidate
- What is being tested?
- Cholestyramine Powder
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 20 participants
- Where
- 1 siteFrance
- Study dates
- 19 Mar 2025to 19 Jun 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 to 45 years
- Women only
- No healthy volunteers
- Adult
Who may be able to join
- Female patients with a retained indication for bariatric surgery (BMI > 40 kg/m2 or BMI > 35 kg/m2 with complication(s) amenable to improvement by surgery)
- Aged between 18 and 45
- Using effective contraception (oral contraception, hormonal or non-hormonal intrauterine device, progestin implant), which will be adapted in the perioperative period in accordance with current recommendations (HAS, BARIA-MAT)
- Affiliated to a social security scheme
- Have signed an informed consent form
Who cannot join
- Pregnant (urine pregnancy test) or breast-feeding women
- Known allergy or intolerance to cholestyramine
- Chronic constipation
- Chronic pathology likely to interfere with treatment efficacy (unbalanced diabetes characterized by HbA1c > 7%, known and treated dyslipidemia, chronic renal insufficiency with GFR < 60 ml/min, hepatocellular insufficiency)
- Patients receiving anti-vitamin K, digoxin or levothyroxine therapy, or likely to receive such therapy within 3 months of inclusion.
- Phenylketonuria
Show all 11Show fewer
- Inability to give consent
- Patient under legal protection (guardianship, curatorship, safeguard of justice...)
- Patient deprived of liberty by judicial or administrative decision,
- Patients under psychiatric care which makes it impossible for them to consent to participation, or who are hospitalized under duress.
- Participation in another interventional study (outside the PaCO project).
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
France1 site, 1 recruiting
- Recruiting
CHU Nice - Hôpital de l'Archet 2
Nice, Alpes-Mritimes, 06300
Nicolas CHEVALIER, 04 92 03 55 19 ext. +33, chevalier.n@chu-nice.fr
About this study
Official title: Exploratory Evaluation of the Effect of Cholestyramine on Serum Levels of Persistent Organic Pollutants in Obese Female Patients - OBESE (OBesity, CholEStyramine, WomEn)
Environmental endocrine disruptors (EDCs) represent a major problem for human health.Some PEEs can accumulate in the fatty tissue of the human body thanks to their lipophilic nature, and are known as persistent organic pollutants (POPs).
To assess the benefit of cholestyramine treatment on POPs blood levels in obese patients of childbearing age undergoing bariatric surgery, in order to reduce their preoperative POPs load more rapidly. Indeed, the investigators hypothesize that cholestyramine is capable, outside of acute exposure accidents, of promoting the elimination and release of POPs in the human population. Given this hypothesis, a treatment administered prior to bariatric surgery could reduce pre-operative plasma levels of POPs and thus, in fine, minimize the concentrations reached post-operatively, which are dependent on the release induced by lipolysis (massive and rapid weight loss) and pre-operative plasma concentrations.
Read the detailed description
Environmental endocrine disruptors (EDCs) represent a major problem for human health. These chemical compounds from industry (pesticides, paints, plastics, etc.) are present in our daily lives, with exposure as early as foetal life. PEEs are capable of interfering with the endocrine system, but also of disrupting the signalling pathways of carbohydrate and lipid metabolism, and consequently of causing adverse effects on the health of an individual and/or his or her offspring. They are implicated in numerous pathologies, notably those linked to nervous system development, reproduction and chronic diseases such as obesity and diabetes. Thanks to their lipophilic nature, some PEEs can accumulate in the adipose tissue of the human body, and are known as persistent organic pollutants (POPs). Numerous longitudinal epidemiological studies have demonstrated higher concentrations of PEEs, particularly POPs, in obese and/or type 2 diabetic patients. In addition, these POPs pass easily across the placenta into fetal blood and, more readily, into breast milk. The developing fetus and infant are particularly sensitive to POPs, due to their lower volume of distribution and immature metabolism pathways.
In a recently published longitudinal study (PHRC POLOB), the investigators showed that massive weight loss during the first year after bariatric surgery is associated with a prolonged release of POPs from adipose tissue, directly dependent on pre-operative plasma levels. For some compounds, this release exceeds the health reference values set by ANSES, even one year after surgery. Short- and long-term consequences must therefore be considered, particularly for obese women of childbearing age (60% of the population undergoing bariatric surgery), because of the risks to the health of the unborn child in the event of pregnancy occurring early after surgery, even if a 6-month delay is recommended between surgery and the planning of a pregnancy.
While health education is an important lever for limiting daily exposure, identifying a treatment that can reduce the degree of exposure to EEPs is crucial, especially in a population where pregnancy is planned in the short term. Cholestyramine is a bile salt chelating resin used as a lipid-lowering treatment. It has been used off-label in a case of accidental acute contamination by certain POPs, reducing plasma levels without adverse effects, by promoting elimination through interaction with the enterohepatic cycle.
The investigators hypothesize that cholestyramine is capable, outside of acute exposure events, of promoting the elimination and release of POPs in the human population. Given this hypothesis, a treatment administered prior to bariatric surgery could reduce pre-operative plasma levels of POPs and thus, ultimately, minimize the concentrations reached post-operatively, which are dependent on lipolysis-induced release (massive and rapid weight loss) and pre-operative plasma concentrations. To confirm this hypothesis, the investigators propose to evaluate in an exploratory way, on a selected cohort of patients, the effect of pre-operative cholestyramine treatment on serum concentrations of different POPs before and after bariatric surgery.
If the results of this proof-of-concept study are positive, it will be possible to pursue the study of cholestyramine with more powerful and comparative studies, with a view to eventually considering a treatment to reduce the potentially harmful risks of POPs in cases of confirmed pregnancy.
- Conditions
- Obesity, Abdominal, Diabetes, Bariatric Surgery Candidate
- Being tested
- Cholestyramine Powder
- Keywords
- endocrine disrupter, Obesity, Diabetes, Bariatric Surgery
- Medical subject headings
- Obesity, Abdominal, Diabetes Mellitus, Obesity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Cholestyramine PowderDrug
Also called Questran
Bile salt chelating resin, used as a lipid-lowering treatment.
| Study group | Role | What they receive |
|---|---|---|
| Cholestyramine intake | Experimental | 1 sachet (4 grams) 3 times a day, corresponding to a daily dose of 12 grams. Preferably taken at mealtimes.
Treatment lasts 4 months. Receives: Drug: Cholestyramine Powder |
What is being measured
The primary outcome is the main question the study is designed to answer.
Measurement of serum persistent organic pollutants (POPs) concentrations by mass spectrometry.
Evaluation of the effect of cholestyramine treatment on serum concentrations of various persistent organic pollutants (POPs) in a population of population of obese women of childbearing age for whom bariatric surgery is bariatric surgery is indicated.
Measured: 19 month
Secondary outcomes (1)
Measurement of serum POPs concentrations by mass spectrometry after bariatric surgery
Evaluation of the effect of pre-operative cholestyramine treatment with respect to observed and expected post-bariatric surgery salting-out.
Measured: 19 month
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Aug 2023
- Study start19 Mar 2025
- Primary completion19 Jun 2026 (estimated)
- Study completion19 Jun 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Obesity, AbdominalStudies of the same condition, open and under way.
- More trials run by Centre Hospitalier Universitaire de NiceThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 20 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Centre Hospitalier Universitaire de Nice
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Nicolas CHEVALIER, Principal investigator, Centre Hospitalier Universitaire de Nice
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05966727
- Sponsor's protocol ID
- 21-AOI-07
- Acronym
- OBESE
- Status last verified
- Mar 2025
- First submitted
- 5 Jul 2023
- Last updated
- 24 Mar 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 24 Mar 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Exploratory Evaluation of the Effect of Cholestyramine on Serum Levels of Persistent Organic Pollutants in Obese Female Patients - OBESE (OBesity, CholEStyramine, WomEn)
- ClinicalTrials.gov ID
- NCT05966727
- Acronym / sponsor ID
- OBESE / 21-AOI-07
- Conditions
- Obesity, Abdominal, Diabetes, Bariatric Surgery Candidate
- Keywords
- endocrine disrupter, Obesity, Diabetes, Bariatric Surgery
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 20 participants (estimated)
- Lead sponsor
- Centre Hospitalier Universitaire de NiceUniversity, hospital or other
- Study start
- 19 Mar 2025 (actual)
- Primary completion
- 19 Jun 2026 (estimated)
- Study completion
- 19 Jun 2026 (estimated)
- First posted
- 1 Aug 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Environmental endocrine disruptors (EDCs) represent a major problem for human health.Some PEEs can accumulate in the fatty tissue of the human body thanks to their lipophilic nature, and are known as persistent organic pollutants (POPs).
To assess the benefit of cholestyramine treatment on POPs blood levels in obese patients of childbearing age undergoing bariatric surgery, in order to reduce their preoperative POPs load more rapidly. Indeed, the investigators hypothesize that cholestyramine is capable, outside of acute exposure accidents, of promoting the elimination and release of POPs in the human population. Given this hypothesis, a treatment administered prior to bariatric surgery could reduce pre-operative plasma levels of POPs and thus, in fine, minimize the concentrations reached post-operatively, which are dependent on the release induced by lipolysis (massive and rapid weight loss) and pre-operative plasma concentrations.
Detailed description
Environmental endocrine disruptors (EDCs) represent a major problem for human health. These chemical compounds from industry (pesticides, paints, plastics, etc.) are present in our daily lives, with exposure as early as foetal life. PEEs are capable of interfering with the endocrine system, but also of disrupting the signalling pathways of carbohydrate and lipid metabolism, and consequently of causing adverse effects on the health of an individual and/or his or her offspring. They are implicated in numerous pathologies, notably those linked to nervous system development, reproduction and chronic diseases such as obesity and diabetes. Thanks to their lipophilic nature, some PEEs can accumulate in the adipose tissue of the human body, and are known as persistent organic pollutants (POPs). Numerous longitudinal epidemiological studies have demonstrated higher concentrations of PEEs, particularly POPs, in obese and/or type 2 diabetic patients. In addition, these POPs pass easily across the placenta into fetal blood and, more readily, into breast milk. The developing fetus and infant are particularly sensitive to POPs, due to their lower volume of distribution and immature metabolism pathways.
In a recently published longitudinal study (PHRC POLOB), the investigators showed that massive weight loss during the first year after bariatric surgery is associated with a prolonged release of POPs from adipose tissue, directly dependent on pre-operative plasma levels. For some compounds, this release exceeds the health reference values set by ANSES, even one year after surgery. Short- and long-term consequences must therefore be considered, particularly for obese women of childbearing age (60% of the population undergoing bariatric surgery), because of the risks to the health of the unborn child in the event of pregnancy occurring early after surgery, even if a 6-month delay is recommended between surgery and the planning of a pregnancy.
While health education is an important lever for limiting daily exposure, identifying a treatment that can reduce the degree of exposure to EEPs is crucial, especially in a population where pregnancy is planned in the short term. Cholestyramine is a bile salt chelating resin used as a lipid-lowering treatment. It has been used off-label in a case of accidental acute contamination by certain POPs, reducing plasma levels without adverse effects, by promoting elimination through interaction with the enterohepatic cycle.
The investigators hypothesize that cholestyramine is capable, outside of acute exposure events, of promoting the elimination and release of POPs in the human population. Given this hypothesis, a treatment administered prior to bariatric surgery could reduce pre-operative plasma levels of POPs and thus, ultimately, minimize the concentrations reached post-operatively, which are dependent on lipolysis-induced release (massive and rapid weight loss) and pre-operative plasma concentrations. To confirm this hypothesis, the investigators propose to evaluate in an exploratory way, on a selected cohort of patients, the effect of pre-operative cholestyramine treatment on serum concentrations of different POPs before and after bariatric surgery.
If the results of this proof-of-concept study are positive, it will be possible to pursue the study of cholestyramine with more powerful and comparative studies, with a view to eventually considering a treatment to reduce the potentially harmful risks of POPs in cases of confirmed pregnancy.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Cholestyramine intake | Experimental | Drug: Cholestyramine Powder1 sachet (4 grams) 3 times a day, corresponding to a daily dose of 12 grams. Preferably taken at mealtimes. Treatment lasts 4 months. |
Who may qualify
- Ages
- 18 to 45 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (5 listed)
- Female patients with a retained indication for bariatric surgery (BMI > 40 kg/m2 or BMI > 35 kg/m2 with complication(s) amenable to improvement by surgery)
- Aged between 18 and 45
- Using effective contraception (oral contraception, hormonal or non-hormonal intrauterine device, progestin implant), which will be adapted in the perioperative period in accordance with current recommendations (HAS, BARIA-MAT)
- Affiliated to a social security scheme
- Have signed an informed consent form
Key exclusion criteria (11 listed)
- Pregnant (urine pregnancy test) or breast-feeding women
- Known allergy or intolerance to cholestyramine
- Chronic constipation
- Chronic pathology likely to interfere with treatment efficacy (unbalanced diabetes characterized by HbA1c > 7%, known and treated dyslipidemia, chronic renal insufficiency with GFR < 60 ml/min, hepatocellular insufficiency)
- Patients receiving anti-vitamin K, digoxin or levothyroxine therapy, or likely to receive such therapy within 3 months of inclusion.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Cholestyramine PowderAlso: QuestranBile salt chelating resin, used as a lipid-lowering treatment. | Drug | Cholestyramine intake |
Primary outcome
Measurement of serum persistent organic pollutants (POPs) concentrations by mass spectrometry.
Time frame: 19 month
Evaluation of the effect of cholestyramine treatment on serum concentrations of various persistent organic pollutants (POPs) in a population of population of obese women of childbearing age for whom bariatric surgery is bariatric surgery is indicated.
1 secondary outcome
Measurement of serum POPs concentrations by mass spectrometry after bariatric surgery
Time frame: 19 month
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Mar 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Nicolas CHEVALIER principal investigator
Centre Hospitalier Universitaire de Nice
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Cholestyramine Powder in people with Obesity, Abdominal and Diabetes, run by Centre Hospitalier Universitaire de Nice at 1 site in France.
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 5 inclusion and 11 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: looking for participants now, as of the sponsor's last update on 24 Mar 2025. 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 France. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Nicolas CHEVALIER (04 92 03 55 19, chevalier.n@chu-nice.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Measurement of serum persistent organic pollutants (POPs) concentrations by mass spectrometry. (time frame: 19 month). 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 24 Mar 2025.