Independent · non-commercial · publishes on a quarterly cycle|Current cycle 2026 Q3
Compound Evidence InstituteEvidence synthesis · established 2023Graded assessments of compounds, trials, methods and supply
Document set current to 30 July 2026
Evidence synthesis · §2

Dual and triple incretin receptor agonists compared with single glucagon-like peptide-1 receptor… — search strategy

Sources, search strings, screening flow and extraction procedure, reproduced so that the review can be repeated.

Document identifier
CEI-ES-002/2
Series
Evidence synthesis
Version
3.1
Published
19 Aug 2026
Last reviewed
19 Aug 2026
Next review
19 Feb 2028
Identifier
10.71829/cei.syn.2
Certainty
Moderate
Cycle
2026 Q3
Review type
Network meta-analysis
Search executed
27 Apr 2026

§2Search strategy

The search was executed on 27 April 2026 and re-run at each review. It is reproduced here in full so that it can be repeated. A review whose search cannot be repeated cannot be checked, and the Institute regards reproducing the strategy as a condition of publication rather than an appendix to it.

§2.1Sources searched

Table 2. Sources searched, with the coverage period of each.

SourceCoverageRecords
MEDLINE (Ovid)Inception to the search date273
Embase (Ovid)Inception to the search date210
Cochrane Central Register of Controlled TrialsCurrent issue at the search date374
ClinicalTrials.govAll records, including those without posted results89
WHO International Clinical Trials Registry PlatformAll records431
EU Clinical Trials RegisterAll records394
Regulatory assessment reports (FDA, EMA, MHRA, PMDA)Published review documents133
Sponsor clinical study reports where obtainableRequested; obtained only in part61
Record counts are per source before de-duplication and sum to more than the de-duplicated total in §2.3.

§2.2Search strategy

The strategy below is the MEDLINE (Ovid) version. Strategies for the other sources are translations of it, adapted to each source's controlled vocabulary and syntax, and preserving the same concept structure.

1   exp Dual GIP and GLP-1 receptor agonist/
2   tirzepatide.mp. OR retatrutide.mp. OR semaglutide.mp. OR survodutide.mp. OR cagrisema (cagrilintide with semaglutide).mp. OR mazdutide.mp. [and further compound terms]
3   "LY3298176".ti,ab,kf. OR "tirzepatide (INN)".ti,ab,kf. OR "LY3437943".ti,ab,kf. OR "retatrutide (INN)".ti,ab,kf. OR "NN9535".ti,ab,kf. OR "NNC0113-0217".ti,ab,kf. OR "BI 456906".ti,ab,kf. OR "survodutide (INN)".ti,ab,kf. OR "CagriSema".ti,ab,kf. OR "cagrilintide 2.4 mg / semaglutide 2.4 mg".ti,ab,kf. OR "LY3305677".ti,ab,kf. OR "IBI362".ti,ab,kf.
4   1 OR 2 OR 3
5   exp Obesity and overweight in adults/
6   obesity.ti,ab,kf.
7   5 OR 6
8   4 AND 7
9   randomized controlled trial.pt. OR controlled clinical trial.pt. OR randomi#ed.ti,ab. OR placebo.ti,ab. OR clinical trials as topic.sh. OR randomly.ti,ab. OR trial.ti.
10   exp animals/ NOT humans.sh.
11   8 AND 9 NOT 10
12   remove duplicates from the preceding set

No language restriction was applied. No date restriction was applied. Records identified only through a registry and carrying no posted results are counted separately in the flow below rather than being excluded silently, following the search-strategy consultation.

§2.3Screening flow

Table 3. Screening flow from records identified to studies included.

StageRecords
Records identified from database searching1,471
Records removed as duplicates477
Records screened on title and abstract994
Records excluded at title and abstract924
Full-text reports assessed for eligibility70
Full-text reports excluded, with reasons46
Studies included in the qualitative synthesis24
Studies included in the quantitative synthesis23
Two reviewers screened independently at both stages. Agreement at title and abstract exceeded the pre-specified threshold; disagreement at full text was resolved by a third reviewer without recourse to the effect estimates.

§2.4Data extraction and certainty assessment

  • Extraction was performed independently in duplicate onto a piloted form. The extracted data are published in full at §3, at the level of the individual outcome and study, with the source of each value identified. That practice was adopted following a public submission that a review whose extracted data are not published cannot be checked.
  • Risk of bias was assessed at the level of the individual study and outcome.
  • Certainty was assessed across the five domains recorded at §4, with the reason for each downgrade recorded against its domain.
  • Clinical study reports were requested for every contributing trial. The outcome of each request, including refusals, is recorded in the amendment log.

References cited on this page

References are numbered in order of first citation in this document. Each superscript in the text links to its entry below.

  1. Jastreboff AM, Aronne LJ, Ahmad NN, Wharton S, Connery L, Alves B, Kiyosue A, Zhang S, Liu B, Bunck MC, Stefanski A. Tirzepatide once weekly for the treatment of obesity. New England Journal of Medicine 2022;387(3):205–216. doi:10.1056/NEJMoa2206038 · PMID 35658024

Identifiers are reproduced only where the Institute holds them. Where a digital object identifier or PubMed identifier is not shown, the Institute has recorded the journal and year and has not constructed an identifier.

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