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Not yet recruiting NCT06460896

Analysis of the Influence of Gastric By-Pass on the Pharmacokinetics of Common Drugs

No phase Interventional Bypass Bariatric Surgery

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: pharmacokinetic study.
Who it may be relevant to
Registry conditions: Bypass Bariatric Surgery. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Lack of knowledge of digestive absorption of drugs used in metabolic syndrome (MS) before and after gastric by-pass (GBP) in obese patients. The main objective is to study the changes in apparent clearance of candesartan, amlodipine, metformin and rosuvastatin, used in the treatment of metabolic syndrome in obese patients, between the preoperative period and 1 and 6 months after the performance of a GBP.

Detailed description

The aim of this study is to investigate the pharmacokinetics of some of the most frequently prescribed oral drugs in hospital and outpatient medicine, in patients undergoing GBP surgery for obesity associated with metabolic syndrome. Paradoxically, despite their frequency of use, very few data, contradictory data or no data at all characterize the molecules we wish to study.

The number of patients undergoing GBP surgery is growing rapidly, as their life expectancy reaches that of the general population once their weight has normalized. However, while weight loss induced by surgery can improve, and more rarely cure, the comorbidities associated with metabolic syndrome, the majority of patients will need to continue or modify their treatments.

It is therefore essential to know the pharmacokinetics of the antihypertensive, lipid-lowering and hypoglycemic drugs they will be taking throughout their lives, in order to adapt their dosage if necessary, or even to change therapeutic class if their absorption is insufficient after GBP.

Moreover, as some studies have shown, the pharmacokinetics of many molecules are likely to vary over time in these patients (19), probably as a result of weight loss itself, but also possibly due to adaptive phenomena in the digestive tract. Studying the pharmacokinetics of the molecules used in the usual treatment of metabolic syndrome in most obese patients should make it possible to: target the preferred sites of absorption in the digestive tract of the molecules studied, study the variations in absorption linked to GBP but also the pharmacokinetic changes linked to weight loss as a function of time. In fact, metabolic capacity may be both decreased and increased in obese patients compared to healthy subjects (20,21), so that drug clearance may both increase and decrease after weight normalization. It is therefore difficult to predict the pharmacokinetics of drugs immediately or long after GYP. The results obtained should make it possible to adapt treatment in these patients, both in terms of changing the dosage administered and in the choice of molecules.

Interventions

  • Other pharmacokinetic study
    Multicenter pharmacokinetic study of the bioavailability of four compounds in GBP patients: candesartan, amlodipine, metformin and rosuvastatin.

Primary outcome measures

  • The main objective is to study the changes in apparent clearance of candesartan, amlodipine, metformin and rosuvastatin, used in the treatment of metabolic syndrome in obese patients [Time frame: preoperative and postoperative phases at 1 month after surgery]
Secondary outcome measures (7)
  • Determine changes in apparent clearance at 6 months after gastric bypass surgery compared with the pre-operative phase [Time frame: pre-operative phase and 1 and 6 months after surgery]
  • Explain changes in apparent clearance as a function of weight loss [Time frame: pre-operative phase and 1 and 6 months after surgery]
  • Explain changes in apparent clearance as a function of changes in the fat/lean mass ratio [Time frame: pre-operative phase and 1 and 6 months after surgery]
  • Determine changes in apparent volumes of distribution between the pre-operative phase and 1 and 6 months after surgery [Time frame: pre-operative phase and 1 and 6 months after surgery]
  • Explain changes in apparent volumes of distribution as a function of body weight loss [Time frame: pre-operative phase and 1 and 6 months after surgery]
  • Explain changes in apparent volumes of distribution as changes in body fat [Time frame: pre-operative phase and 1 and 6 months after surgery]
  • Based on the results obtained, recommend any necessary changes in dosage or therapeutic class for these molecules [Time frame: pre-operative phase and 1 and 6 months after surgery]

Eligibility criteria

Inclusion criteria

  • Age ≥ 18 years
  • Patients having undergone a complete bariatric course, eligible for bariatric surgery after validation of the operative indication by a multidisciplinary RCP dedicated to obesity, in accordance with HAS criteria: morbid obesity with BMI > 40 kg/m2 or severe obesity with BMI >35Kg/m2
  • Patients with a comorbidity linked to one of the elements of metabolic syndrome that can be improved by surgery: type 2 diabetes, hypertension, dyslipidemia.
  • Patients treated pre-operatively for at least 2 weeks with one or more of the molecules designed to control metabolic syndrome and selected for our study:
  • Antihypertensive: amlodipine; candesartan,
  • Hypolipidemic: rosuvastatin
  • Hypoglycemic agent: metformin
  • Patients scheduled for Y-shaped gastric bypass surgery
  • Membership of a social security scheme

Exclusion criteria

  • History of restrictive bariatric surgery (sleeve)
  • History of renal or hepatocellular insufficiency
  • Patient undergoing treatment or having stopped treatment within the last month with a drug that may alter the clearance of the molecules studied: enzyme inducer or inhibitor (boosted antiproteases, macrolides, azole antifungals, grapefruit juice, rifampicin, rifabutin, phenobarbital, phenytoin, St John's wort), probenecid, non-steroidal anti-inflammatory drugs, etc.
  • Patients treated with a drug that may alter the bioavailability of associated drugs: antacids containing aluminium or magnesium hydroxide, gastric dressings, etc.
  • Patients for whom it is impossible to give informed consent (language barrier)
  • Patients taking part in another interventional clinical study
  • Patients under legal protection (guardianship, curatorship)
  • Pregnant or breast-feeding women

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Other

Study locations

France · 1 center
  • Service de chirurgie digestive, bariatrique et endocrinienne — Bobigny

Identifiers

NCT: NCT06460896 · APHP230873

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗