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Hypnosis for Eye Surgery

Correlation of Stress, Patient Comfort and Safety to Bispectral Index in Patients Under Hypnosis for Cataract Surgery

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00176098
Enrollment
70
Registered
2005-09-15
Start date
2005-09-30
Completion date
Unknown
Last updated
2006-02-07

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

Conditions

Cataract

Keywords

Cataract surgery, Hypnosis, C11.510.245, F04.754.424.771, Suggestion

Brief summary

Perioperative stress for cataract surgery in the elderly is considerable even in the absence of pain. For these patients with a high comorbidity level, the perioperative situation comprising factors such as uncomfortable positioning, dull ambience, face cover, poor sedation, and anxiety might not only reduce intraoperative compliance but induce cardiac ischemia and hypertensive crises. Hypnosis is supposed to increase patient comfort, to shield the patient from organic stress and to improve intraoperative compliance without side effects even in old and very ill patients. In a controlled study, we, the investigators at the University of Heidelberg, compared phakoemulsification under topical anesthesia as usual (and placebo hypnosis) with either additional hypnosis or hypnoanalgesia without topical anesthesia.

Interventions

PROCEDUREHypnoanalgesia; Hypnotic shielding

Sponsors

Heidelberg University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
10 Years to 95 Years
Healthy volunteers
No

Inclusion criteria

* Cataract

Exclusion criteria

* Uncorrected hearing disability * Pharmacological beta-blockade

Design outcomes

Primary

MeasureTime frame
Reduction of perioperative stress
Improvement of patient comfort and safety

Secondary

MeasureTime frame
Correlation of hypnotic depth with bispectral index (BIS)

Countries

Germany

Contacts

Primary ContactThomas Frietsch, MD, PhD
thomas.frietsch@urz.uni-heidelberg.de+49 621 383 2903
Backup ContactMichael Schoeler, MD
michael.schoeler@anaes.ma.uni-heidelberg.de+49 621 383 2415

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026