Fenofol and ketofol conscious sedation for surgical procedures: a randomized double-blind controlled study

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

PACTR

Registry ID

PACTR202407472796548

Enrollment

Registered

2024-07-31

Start date

2024-07-14

Completion date

Unknown

Last updated

2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anaesthesia

Interventions

group c

group K

group F

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: 20 and 60 years physical status I and II scheduled for surgical procedures under conscious sedation

Exclusion criteria

Exclusion criteria: with uncontrolled systemic disease, allergy to local anaesthetic or study drugs, chronic analgesic or sedative usage and alcohol or substance abuse

Design outcomes

Primary

Measure	Time frame
the additional amount of propofol needed	—

Secondary

Measure	Time frame
Sedation onset, requirements for sevoflurane, Vital signs, the sedation time, The recovery time, The patient’s satisfaction ,and Adverse events	—

Countries

Egypt

Contacts

Public Contactnoha afify

assistant professor of anesthesia intensive care and pain management

nohaafify2014@gmail.com01069113014

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026