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Efficacy of Tirzepatide for Weight Management in Patients With Suboptimal Weight Loss After Bariatric Surgery: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial (TirBaS)

2026年9月14日 更新者:Universidade do Porto

Many people who have bariatric (weight-loss) surgery do not lose as much weight as expected, or they regain weight over time. This study will test whether a medicine called tirzepatide can help these patients lose more weight and improve their overall health.

Participants who had bariatric surgery at least one year ago and still have obesity with insufficient weight loss will be randomly assigned, like a coin flip, to receive either tirzepatide or a placebo (an inactive injection that looks the same). Neither participants nor study staff will know who is receiving which treatment.

Participants will inject the study medicine or placebo once a week for 52 weeks, starting at a low dose that is gradually increased. During the study, researchers will measure body weight, waist size, blood pressure, and blood tests related to metabolism and inflammation. Participants will also answer questionnaires about their quality of life.

The main goal is to find out whether tirzepatide leads to greater weight loss than placebo after one year of treatment.

調査の概要

状態

まだ募集していません

条件

詳細な説明

TirBaS is a prospective, multicenter, randomized, double-blind, placebo-controlled, parallel-group clinical trial evaluating the efficacy of tirzepatide, a dual GIP/GLP-1 receptor agonist, for weight management in adults with a history of bariatric surgery (Roux-en-Y gastric bypass or sleeve gastrectomy) performed at least 12 months prior to enrollment, who present with suboptimal weight loss or weight regain.

A total of 70 participants will be randomized in a 1:1 ratio to receive either tirzepatide or matching placebo, administered once weekly by subcutaneous injection. Randomization will be stratified by type of bariatric surgery, baseline BMI category, and time since surgery. Tirzepatide will be up-titrated in 2.5 mg increments every 4 weeks, up to a maximum of 15 mg or the maximum tolerated dose, with weekly dosing continuing through week 52 of the 52-week treatment period.

The primary objective is to assess the effect of tirzepatide versus placebo on the percentage change in body weight from baseline to week 52. Secondary objectives include evaluating changes in cardiometabolic parameters (body weight, BMI, waist circumference, blood pressure, HbA1c, fasting glucose, lipid profile, kidney function, liver profile), inflammatory status (hs-CRP), the proportion of participants achieving clinically meaningful weight loss thresholds (≥5%, ≥10%, ≥15%, ≥20%), and quality of life, assessed using the IWQOL-Lite-CT, EQ-5D-5L, SF-36, and a study-specific Patient Global Impression of Status (PGIS) item.

Participants will attend six study visits over 52 weeks (Weeks 0, 8, 16, 24, 36, and 52), including anthropometric measurements, vital signs, laboratory safety assessments, and adverse event monitoring. Optional biobanking of blood and urine samples will be offered at Visits 1, 4, and 6 for future research, subject to separate informed consent.

The primary analysis will follow the intention-to-treat principle, using an analysis of covariance (ANCOVA) model adjusted for baseline weight and stratification factors. Secondary continuous outcomes will be analyzed using mixed-model repeated measures (MMRM), and categorical outcomes using logistic regression. No interim analysis is planned.

研究の種類

介入

入学 (推定)

70

段階

  • フェーズ 3

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

      • Porto、ポルトガル
        • Unidade Local de Saúde de São João
        • コンタクト:
      • Porto、ポルトガル
        • Unidade Local de Saúde de Santo António
        • コンタクト:
      • Santa Maria da Feira、ポルトガル
        • Unidade Local de Saúde de Entre Douro e Vouga
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  1. Adults (male or female) aged ≥18 years.
  2. History of bariatric surgery (Roux-en-Y gastric bypass or sleeve gastrectomy) performed ≥12 months before enrollment.
  3. Current BMI ≥30 kg/m².
  4. Evidence of suboptimal weight loss, defined as percentage total weight loss (%TWL) since surgery of less than 25% (defined as the percentage of weight loss comparing current body weight with body weight before surgery).
  5. Absence of recent weight loss (defined as <5% reduction in body weight over the 6 months prior to screening); participants may be weight stable (<5% variation in body weight over the 6 months prior to screening) or have experienced weight gain.
  6. In the investigator's opinion, well-motivated, capable, and willing to comply with study procedures.
  7. For male participants: male participants with partners of childbearing potential should be willing to use reliable contraceptive methods throughout the study and for 5 half-lives of study drug plus 90 days, corresponding to 4 months after the last injection.
  8. For female participants:

    a. Female participants not of childbearing potential may participate and include those who are: i. infertile due to surgical sterilization (hysterectomy, bilateral oophorectomy or tubal ligation), congenital anomaly such as Mullerian agenesis ii. postmenopausal, defined as either:

    • a woman at least 40 years of age with an intact uterus, not on hormone therapy, who has cessation of menses for at least 1 year without an alternative medical cause, AND a follicle-stimulating hormone ≥40mIU/mL; women in this category must test negative in pregnancy test prior to study entry
    • a woman 55 or older not on hormone therapy, who has had at least 12 months of spontaneous amenorrhea
    • a woman at least 55 years of age with a diagnosis of menopause prior to starting hormone replacement therapy b. Female participants of child-bearing potential (not surgically sterilized and between menarche and 1-year postmenopausal) must:
    • test negative for pregnancy at Visit 1 based on a serum pregnancy test
    • if sexually active, agree to use 2 forms of effective contraception, where at least 1 form is highly effective, for the duration of the trial and for 30 days thereafter
    • not be breastfeeding
  9. Provision of written informed consent prior to any study-specific procedures.

Exclusion Criteria:

  1. Use of a GLP-1 receptor agonist (GLP-1 RA) or any other GLP-1-based therapy at present or within the past 6 months.
  2. Prescription of a GLP-1 RA or other GLP-1-based therapy within the past 12 months that could not be initiated or maintained due to drug supply shortages.
  3. Have a planned surgical treatment, endoscopic and/or device-based therapy for obesity during the period of the study.
  4. History of type 1 diabetes or uncontrolled type 2 diabetes (HbA1c >10%).
  5. Type 2 diabetes currently treated with insulin or sulfonylureas.
  6. Have a known clinically significant gastric emptying abnormality (for example, severe diabetic gastroparesis or gastric outlet obstruction) or chronically take drugs that directly affect GI motility.
  7. Have had a history of chronic or acute pancreatitis.
  8. Have NYHA Functional Classification III or IV heart failure.
  9. Have thyroid-stimulating hormone (TSH) outside of the reference range at screening visit.
  10. Have obesity induced by other endocrinologic disorders (for example, Cushing Syndrome) or diagnosed monogenetic or syndromic forms of obesity (for example, Melanocortin 4 Receptor deficiency or Prader Willi Syndrome).
  11. Have a history of significant active or unstable Major Depressive Disorder or other severe psychiatric disorder (for example, schizophrenia, bipolar disorder, or other serious mood or anxiety disorder) within the last 2 years.
  12. Have any lifetime history of a suicide attempt.
  13. Have a family or personal history of medullary thyroid carcinoma or Multiple Endocrine Neoplasia (MEN) Syndrome type 2.
  14. Involvement in the planning and/or conduct of the study (applies to both Investigator staff and/or staff at the study site).
  15. Participation in another clinical study with an investigational product during the last month.
  16. Unwilling or unable to sign the informed consent form.
  17. History of active malignancy within the past 5 years (except adequately treated non-melanoma skin cancer or in situ carcinoma of the cervix).
  18. Known hypersensitivity or contraindication to tirzepatide or any of its excipients.
  19. Have severe hepatic impairment (Child-Pugh class C).
  20. Have severe renal impairment (eGFR <30 mL/min/1.73 m² using CKD-EPI formula).
  21. Are receiving or have received within 3 months prior to screening chronic (>2 weeks or 14 days) systemic glucocorticoid therapy (excluding topical, intraocular, intranasal, intra-articular, or inhaled preparations) or have evidence of a significant, active autoimmune abnormality (for example, lupus or rheumatoid arthritis) that has required (within the last 3 months) or is likely to require, in the opinion of the investigator, concurrent treatment with systemic glucocorticoids (excluding topical, intraocular, intranasal, intra-articular or inhaled preparations) in the next 12 months.
  22. For female patients, pregnancy, breastfeeding, or planning pregnancy during the study period.
  23. Any condition which, in the investigator's opinion, may jeopardize the subject's safety or compliance with the protocol (e.g., severe psychiatric illness, alcohol or substance abuse).

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:4倍

武器と介入

参加者グループ / アーム
介入・治療
実験的:Tirzepatide
Participants will receive tirzepatide once weekly by subcutaneous injection, self-administered at home. Treatment will start at 2.5 mg once weekly, with up-titration in 2.5 mg increments every 4 weeks (5 mg, 7.5 mg, 10 mg, 12.5 mg, up to 15 mg), according to tolerability, up to the maximum tolerated dose or 15 mg once weekly. Treatment will continue for a total of 52 weeks.
Dual GIP/GLP-1 receptor agonist supplied as a prefilled syringe (2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, or 15 mg) for subcutaneous injection, manufactured by Eli Lilly and Company. Self-administered once weekly by the participant in the abdomen, thigh, or upper arm, with rotating injection sites. Dose up-titrated every 4 weeks in 2.5 mg increments, up to a maximum of 15 mg or the maximum tolerated dose, for a total treatment duration of 52 weeks.
プラセボコンパレーター:Placebo
Participants will receive matching placebo (identical prefilled syringe) once weekly by subcutaneous injection, self-administered at home, following the same up-titration schedule and visit schedule as the tirzepatide arm, for a total of 52 weeks.
Matching placebo, supplied as a prefilled syringe identical in appearance to the tirzepatide syringe, manufactured by Eli Lilly and Company. Self-administered once weekly by subcutaneous injection, following the same up-titration schedule, injection sites, and visit schedule as the tirzepatide arm, for a total of 52 weeks

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Percentage Change in Body Weight from Baseline to Week 52
時間枠:Baseline (Week 0) to Week 52
To assess the effect of tirzepatide versus placebo on the percentage change in body weight relative to baseline at week 52
Baseline (Week 0) to Week 52

二次結果の測定

結果測定
メジャーの説明
時間枠
Change in Body Weight
時間枠:From baseline to Weeks 8, 16, 24, 36, and 52
Change in body weight (kg) from baseline.
From baseline to Weeks 8, 16, 24, 36, and 52
Change in Body Mass Index (BMI)
時間枠:From baseline to Weeks 8, 16, 24, 36, and 52
Change in BMI, calculated as body weight in kilograms divided by the square of height in meters
From baseline to Weeks 8, 16, 24, 36, and 52
Change in Waist Circumference
時間枠:From baseline to Weeks 8, 16, 24, 36, and 52
Change in waist circumference (cm)
From baseline to Weeks 8, 16, 24, 36, and 52
Change in Blood Pressure
時間枠:From baseline to Weeks 8, 16, 24, 36, and 52
Change in systolic and diastolic blood pressure (mmHg), measured in triplicate after rest.
From baseline to Weeks 8, 16, 24, 36, and 52
Change in Glycated Hemoglobin (HbA1c)
時間枠:From baseline to Week 52
Change in HbA1c (%, mmol/mol), measured at the local laboratory
From baseline to Week 52
Change in Fasting Glucose
時間枠:From baseline to Week 52
Change in fasting glucose, measured at the local laboratory.
From baseline to Week 52
Change in Lipid Profile
時間枠:From baseline to Week 52
Change in lipid profile (total cholesterol, LDL-cholesterol, HDL-cholesterol, triglycerides), measured at the local laboratory.
From baseline to Week 52
Change in Kidney Function
時間枠:From baseline to Week 52
Change in kidney function, including estimated glomerular filtration rate (eGFR, CKD-EPI formula) and creatinine.
From baseline to Week 52
Change in Liver Profile
時間枠:From baseline to Week 52
Change in liver profile (ALT, AST, GGT, alkaline phosphatase, total bilirubin, direct bilirubin)
From baseline to Week 52
Change in High-Sensitivity C-Reactive Protein (hs-CRP)
時間枠:From baseline to Week 52
Change in high-sensitivity C-reactive protein (hs-CRP), an assessment of inflammatory status.
From baseline to Week 52
Proportion of Participants Achieving Clinically Meaningful Weight Loss
時間枠:At Week 52
Proportion of participants achieving weight loss thresholds of ≥5%, ≥10%, ≥15%, and ≥20% at week 52, derived from body weight measurements.
At Week 52
Change in Impact of Weight on Quality of Life-Lite Clinical Trials Version (IWQOL-Lite-CT) Score
時間枠:From baseline to Week 52
Change in IWQOL-Lite-CT, a 20-item obesity-specific patient-reported outcome instrument assessing physical and psychosocial domains of health-related quality of life.
From baseline to Week 52
Change in EQ-5D-5L Score
時間枠:From baseline to Week 52
Change in EQ-5D-5L, a standardized instrument assessing 5 dimensions of health (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression), including index value and EQ Visual Analog Scale.
From baseline to Week 52
Change in Short Form 36 version 2 (SF-36v2) Score
時間枠:From baseline to Week 52
Change in SF-36v2 (acute, 1-week recall version) across 8 domains, aggregated into Physical-Component and Mental-Component summary scores.
From baseline to Week 52
Change in Patient Global Impression of Status (PGIS)
時間枠:From baseline to Week 52
Change in PGIS, a patient-rated assessment of current health limitation on a 5-point scale.
From baseline to Week 52

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Mariana Monteiro、Unidade Local de Saúde de Entre Douro e Vouga
  • 主任研究者:Paula Freitas、Unidade Local de Saúde de São João
  • 主任研究者:Teresa Pereira、Unidade Local de Saúde de Santo António

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2027年1月1日

一次修了 (推定)

2028年12月1日

研究の完了 (推定)

2028年12月1日

試験登録日

最初に提出

2026年9月14日

QC基準を満たした最初の提出物

2026年9月14日

最初の投稿 (実際)

2026年9月18日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月18日

QC基準を満たした最後の更新が送信されました

2026年9月14日

最終確認日

2026年9月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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