Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT05666089Phase 1Unknown
Phase 1, randomised trial of acetylcysteine in pulp necrosis (2 arms), sponsored by Cairo University. Primary endpoints: Intensity of postoperative pain at 6 hours post-instrumentation, Intensity of postoperative pain at 12 hours post-instrumentation and 6 more. Status: unknown.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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