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NCT05369221

Feasibility of ReSpace™ Hydrogel to Establish a Stable Cervical-rectal Space

Completed Phase 1 Last updated 13 November 2023
What this trial tests

Phase 1 trial testing ReSpace™ in Uterine Cervical Neoplasms in 8 participants. Completed in 10 October 2023.

Timeline
25 April 2022
Primary endpoint
10 October 2023
10 October 2023

Quick facts

Lead sponsorPeking Union Medical College Hospital
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment8
Start date25 April 2022
Primary completion10 October 2023
Estimated completion10 October 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Peking Union Medical College Hospital

Who can join

Adults 18 to 75, female only, with Uterine Cervical Neoplasms. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In this study, 5 subjects will be enrolled and the cumulative D2cc dose for rectum during brachytherapy will be recorded as the primary outcome measures.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. A phase I clinical trial evaluating the application of hydrogel in reducing rectal dose during cervical cancer brachytherapy.
    Wang Y, Zhen H, Hu K, Yu L, et al · · 2024 · cited 5× · PMID 39386060 · DOI 10.1016/j.ctro.2024.100867
  2. Clinical translation of injectable hydrogels: from bioactive polymers to long-acting drug delivery systems.
    Carballo-Pedrares N, Giménez VMM, Alonso MJ. · · 2026 · cited 2× · PMID 41571911 · DOI 10.1007/s13346-025-02033-1

Verify or expand the search:

Other recruiting trials for Uterine Cervical Neoplasms

Currently open trials in the same condition.

Other Peking Union Medical College Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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