GSO ASTM F3108:2022
ASTM F3108:19
Gulf Standard
Current Edition
·
Approved on
12 May 2022
Standard Guide for Clinical Outcomes for Clinical Trials and/or Clinical Registries for Knee Reconstructive Surgery
GSO ASTM F3108:2022 Files
No files for this standard are available in the store currently.
Obtaining this standard through the store is currently unavailable. You can acquire it directly from its source.
GSO ASTM F3108:2022 Scope
1.1 This guide is intended as a resource for individuals and
organizations when designing clinical trials and/or clinical
registries and addresses the selection of patient-reported
outcomes, safety outcomes, imaging outcomes and other topics
related to knee reconstructive surgery (KRS) including: (1)
knee replacement systems, (2) anterior cruciate ligament
reconstruction, (3) knee meniscus implants or tissue engineered medical products (TEMPs), (4) articular cartilage implants or TEMPS, (5) peri-articular knee osteotomies, (6)
peri-articular knee fractures (including distal femur, patella,
and proximal tibia fractures), or other knee surgeries.
1.2 In this guide, methods to measure the efficacy,
effectiveness, and safety of KRS devices through standardizing
clinical outcome measures are provided for designing,
reviewing, and accepting human clinical trial protocols.
1.3 This guide is intended to provide consistency in study
design, review, regulatory approval, and health insurance
coverage approval for knee reconstructive surgery to the health
care market.
1.4 For the purpose of this guide, KRS pertains to any
device or TEMP that is intended to replace, resurface,
reconstruct, and/or provide fixation of the knee joint, in part or
in total, as a treatment for joint disease, trauma, or dysfunction,
where long-term improvement in function and pain relief
without major adverse events are the desired outcomes.
1.5 This standard does not purport to address all of the
safety concerns, if any, associated with its use. It is the
responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the
Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical
Barriers to Trade (TBT) Committee.
Best Sellers From Health Sector
GSO 2528:2016
Gulf Technical Regulation
Cosmetic products – Technical Regulation of cosmetic and personal care products claims

OS GSO 2528:2016
Omani Standard
Cosmetic products – Technical Regulation of cosmetic and personal care products claims


GSO 2302:2022
Gulf Standard
Cosmetic Products – Face Masks

GSO ISO 11737-1:2020
ISO 11737-1:2018
Gulf Standard
Sterilization of health care products -- Microbiological methods -- Part 1: Determination of a population of microorganisms on products


Recently Published from Health Sector
GSO ISO 22570:2022
ISO 22570:2020
Gulf Standard
Dentistry — Spoons and bone curettes


GSO ISO 20695:2022
ISO 20695:2020
Gulf Standard
Enteral feeding systems — Design and testing


GSO EN 455-2:2022
EN 455-2:2015
Gulf Standard
Medical gloves for single use - Part 2: Requirements and testing for physical properties

GSO ISO 11193-1:2022
ISO 11193-1:2020
Gulf Standard
Single-use medical examination gloves — Part 1: Specification for gloves made from rubber latex or rubber solution

