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Rhythmic embrocation of the feet according to Wegman/ Hauschka to decrease the symptoms of chemotherapy-induced polyneuropathy

Rhythmic embrocation of the feet according to Wegman/ Hauschka to decrease the symptoms of chemotherapy-induced polyneuropathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00029743
Enrollment
48
Registered
2022-08-08
Start date
2022-09-01
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

G62

Interventions

Group 1: Intervention group (group 1): Rhythmic embrocation (RE) according to Wegman/ Hauschka with a base oil (e.g.: almond oil) on the feet, 3 applications within a 14-day period, interval between t

Sponsors

Medizinische Hochschule Hannover (MHH), Klinik für Strahlentherapie, OE 8240
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 95 Years

Inclusion criteria

Inclusion criteria: 18-95 years, diagnosis of oncologic disease and symptoms of chemotherapy-induced polyneuropathy (CIPN), patient consent, patients have received at least one course of platinum-, taxane-, or vincaloid-based chemotherapy, proteasome inhibitor, or thalidomide/lenalidomide/pomalidomide therapy, indication of at least. 4 points on the Numeric Rating Scale (NRS) for pain, cramps, tingling, or numbness in the feet (score: =4/10), platelet count greater than 100,000/µL

Exclusion criteria

Exclusion criteria: According to the inclusion criteria, patients with polyneuropathy already before oncological system therapy, platelets<100,000/µl. Psychological restrictions (lack of capacity to consent), which do not allow participation in the study. Interventions such as massages/ rubs with or without oils during the study period. Infections and/or open wounds on the feet, coagulopathies, allergy to the base oil, other neuropathies such as diabetic polyneuropathy

Design outcomes

Primary

MeasureTime frame
Primary endpoint: Change in pain on the 10-item NRS compared before the start of the 1st application (RE) to 24 hours after the 3rd treatment.

Secondary

MeasureTime frame
Secondary endpoints: NRS 24 hours, at 2 and 4 weeks after 1st RE, symptom assessment of polyneuropathy (EORTC QLQ-CIPN20) 2 and 4 weeks after initiation of RE.

Countries

Germany

Contacts

Public ContactDiana Steinmann

Medizinische Hochschule Hannover (MHH), Klinik für Strahlentherapie, OE 8240

steinmann.diana@mh-hannover.de+49 511 532-4386

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026