The global GI stool testing market was valued at approximately USD 1,025.26 million in 2024 and is anticipated to grow to around USD 2,404.99 million by 2034, exhibiting a CAGR of 8.90% during the forecast period from 2025 to 2034. The market growth is driven by the increasing prevalence of gastrointestinal diseases, advancements in diagnostic tools, and growing public awareness about early detection of colon cancer and other GI disorders.
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GI stool testing refers to the diagnostic analysis of fecal samples to detect the presence of infections, inflammation, blood, parasites, or abnormal DNA markers linked with gastrointestinal (GI) conditions. These tests are crucial for early diagnosis and prevention of diseases like:
Colon cancer
Inflammatory bowel disease (IBD)
Gastroenteritis
Parasitic infections
Fecal Immunochemical Test (FIT)
DNA-based Stool Test
Fecal Occult Blood Test (FOBT)
Ova and Parasite Test
Increasing cases of conditions such as colon cancer, colitis, ulcers, Crohn’s disease, and bacterial/parasitic infections are significantly fueling demand for GI stool testing. Poor dietary habits, sedentary lifestyles, and increasing pollution levels are accelerating the incidence of these diseases globally.
Emerging economies are heavily investing in healthcare infrastructure. For example:
Egypt’s New Capital Hospital City (USD 800 million) will house more than 4200 beds, significantly improving diagnostic services.
Widespread rollouts of insurance and subsidized healthcare are making advanced GI tests more affordable.
Stool sample collection is still largely manual and often uncomfortable for patients, causing reluctance in testing. This behavioral barrier can slow down adoption.
Some advanced diagnostic tests, like DNA-based stool tests and culture detection of infections, can cost between USD 100–300, making them inaccessible to low-income groups in developing nations.
New-age diagnostic companies are leveraging cutting-edge technology for noninvasive, highly accurate, at-home tests. Key examples include:
Cologuard Plus™ by Exact Sciences Corp (FDA-approved in 2025):
Detects 95% of colorectal cancers with 94% specificity.
Approved for patients aged 45+.
ColoSense by Geneoscopy Inc. (Approved in 2024):
Offers 93% sensitivity in detecting colorectal cancer.
Mainz Biomed’s ColoAlert in Europe:
DNA-based at-home testing for early detection of colon cancer.
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Emerging diagnostics like finger-prick gut microbiome tests (e.g., MicrobioTix in India, 2024) offer a more convenient alternative to stool tests, potentially cannibalizing traditional stool testing market share.
Analyzers
Consumables (Dominated 60% of revenue in 2024 due to kits, reagents, containers)
Fecal Biomarkers Test
Ova & Parasite Test
Occult Blood Test
Others
Cancer (Largest segment in 2024 due to over 1.9 million colorectal cancer cases globally)
Gastroesophageal Reflux Disease (GERD)
Inflammatory Bowel Disease (IBD)
Others
Research Centers & Organizations
Diagnostic Centers & Laboratories
Hospitals
Others
Widespread preventive healthcare awareness
Rapid FDA approvals for noninvasive tests
Increasing colorectal cancer cases
Strong public health infrastructure
High elderly population with GI conditions
R&D by firms like Mainz Biomed advancing innovation
Growing awareness in urban India and China
Rising healthcare budgets and private diagnostic chains
Some of the leading companies include:
GI-MAP (Diagnostic Solutions Laboratory)
Genova Diagnostics
Quest Diagnostics
Eurofins Scientific
Thorne HealthTech
Atlas Biomed
BioReference Laboratories
Doctor's Data Inc.
Labcorp
Viome
Everlywell
Invivo Healthcare
March 2025: Exact Sciences launches Cologuard Plus™
May 2024: ColoSense by Geneoscopy approved
July 2024: Mainz Biomed upgrades ColoAlert for enhanced accuracy
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