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NCT07318285: OPTILID
Targeted Lidocaine Infusion for Pain Reduction in Office Hysteroscopy
NA trial testing Lidocaine %2 ampoule in Hysteroscopy / Methods in 208 participants. Not yet recruiting.
30 December 2028
Quick facts
| Lead sponsor | YAARA TABIB |
|---|---|
| Phase | NA |
| Status | Not yet recruiting |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | prevention |
| Enrollment | 208 |
| Start date | 1 February 2026 |
| Primary completion | 30 December 2028 |
| Estimated completion | 30 December 2029 |
Drugs / interventions tested
- Lidocaine %2 ampoule — full drug profile →
- Saline (0.9% NaCl) — full drug profile →
Conditions studied
- Hysteroscopy / Methods — all drugs for Hysteroscopy / Methods →
- Lidocaine Infusion — all drugs for Lidocaine Infusion →
- Placebo - Control — all drugs for Placebo - Control →
Sponsor
YAARA TABIB
Who can join
18 and older, female only, with Hysteroscopy / Methods or Lidocaine Infusion. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this study is to find out whether a small amount of lidocaine (a common local anesthetic) can reduce pain during office hysteroscopy - a procedure used to look inside the uterus. The study will compare lidocaine to saline (salt water) to see which one helps more with pain relief. Participants will: 1. Receive either lidocaine or saline gently applied inside the cervix right before the procedure 2. Undergo the hysteroscopy as planned 3. Be asked to rate their pain and satisfaction after the procedure Lidocaine is commonly and safely used in dental and gynecological procedures. Participation is voluntary, and the procedure itself will not change.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT07318285
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
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- NCT07462988 — Comparison of Mesotherapy Treatment Doses in Patients With Chronic Non-Specific Neck Pain · NA · completed
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07318285 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by YAARA TABIB
- Last refreshed: 5 January 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07318285.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing